On Saturday, September 26, 2009 4:28 PM, bagher mohammadpour <bmp1337@yahoo.com> wrote:
Bagher Mohammad Pour,
(Mr, Pharm. D., Tabriz Uni., Iran)
Paris, France.
28.09.2009
Pfizer Inc
Legal Department
235 East 42nd Street
New York, NY 10017
Phone (212) 573-1911
USA
At Pfizer, we're inspired by a single goal: your health.
The first sentence from Pfizer.com/home/Dear Sir Jeffrey B. Kindler
Chief Executive Officer and Chairman of the Board, Pfizer Inc
I
am an Iranian pharmacist with more than twenty years of experience in
the pharmaceutical companies of Iran. You will find soon why I do not
call these collection of factories industry.
According to the currant level of pharmaceutical sciences and technologies and regulations in the modern world, what has been COMMITTING in the name of "manufacturing medicines" in IRAN is a full scale national disaster from a technical, social and Human Rights point of view: a danger from which there is no scape and all and all the members of a Nation are sentenced to its unpredictable consequences for no reason.
I hope your and your colleagues' personal and professional interests and commitment in Pfizer as the biggest manufacturer of pharmaceuticals to the advancement of Human Health and life quality in our professional field help me urgently to bring my lifelong struggle on which I scarified all my life and legitimate social interests to its victorious end in favor of a big Nation who are spending the absolute darkest period of their history.
FDA
and many other professional organizations rejected to declare their
opinion when I asked about their assessment and evaluations of a
pharmaceutical system that is able to do all those HUGE practical and
theoretical mistakes and DISASTERS. They knew completely the meaning of
those mistakes and for fear of leaking their reply to public. Case 3-14
is an example for IMMPOSSIBLE; world will find it everything bu
Today
it is an received opinion and belief, both nationally and
internationally, that: Any commitment to advancement of Human Rights and
Life in Iran must be asserted by deeds, for words, on this subject, it
is a long time, have nearly exhausted their POWER.
1-FROM Tabriz university in Iran I received my Pharm. D. degree
at the beginning of 1985. I have spent all my professional life in
service of the pharmaceutical industries of Iran. From the very first
weeks I faced a lot of huge scientific and practical mistakes in all
aspect of production of medicinals. Unfortunately leaving a company and
joining another only changed my mistrust in inadequacy of theoretical
and practical arrangements into an absolute faith in existence of a
nationwide disaster in these industries.
My DISASTROUS and incredible findings in every company put them in danger of a devastating earthquake with unpredictable consequences not only for themselves but for MoH who carried all and also the final responsibility of everything industries did & DO. So I always forced to move (actually I was dismissed) to another company and repeating the same story.
2-ABOUT fifteen years ago I wrote a long and critical article on this subject but
My DISASTROUS and incredible findings in every company put them in danger of a devastating earthquake with unpredictable consequences not only for themselves but for MoH who carried all and also the final responsibility of everything industries did & DO. So I always forced to move (actually I was dismissed) to another company and repeating the same story.
2-ABOUT fifteen years ago I wrote a long and critical article on this subject but
no
one dared to publish it for having serious consequences on Government’s
legitimacy and would put both the publisher and writer in danger of
harsh reactions of the regime.
3-THE followings are only a short list of those serious mistakes:
3-1 Usage delicate and unstable materials like vitamins five to seven years after the end of their Expiration Dates.
3-2 Huge mistakes in laboratory control methods of Raw Materials and finished products so that mistakes up to fifty percent, and usually more, could not be detected or could be introduced.
3-3 Mixing of raw well water with syrups for too many years because of a design defect in the filling machine.
3-4 correction of a totally wrong manufacturing procedure reduced the manufacturing time from ten hours in tow days to three hours in one day. A further correction of its formulation reduced its excipients about 1300 kg per 3000 l: this means their ignorance put the metabolic system of children under a severe pressure for absolutely no benefit or necessity. Its bitter taste and disgusting smell vanished for ever.
3-5 Defect in installation of a washing machine led to remaining about two milliliters of an extremely concentrated Chlorine water, one of the most dangerous Oxidizing agents, in the washed bottles used for bottling the above mentioned pediatric antibiotic suspension.
3-6 Usage an totally Inactive microbial preservative in an antacid suspension for too many years for the complete ignorance of the most basic principles of chemistry and biology.
3-7 For a while a company introduced a preparation without any Active component (drug molecules) into market for Economical reasons.
3-8 Active ingredient of an antacid suspension and tablets were respectively 25% and 16% less than the label amounts in at least two company.
3-9 In a comprehensive report, in more than one hundred pages, I proved that nearly what I knew till then in that company were wrong to the strongest and widest meaning of the word of wrong.
3-10 And there are too many other cases which I could not mention them for ,at least, the matter of space.
3-11 correction of filtering technique of a sugar syrup prevented the entrance of considerable amount of any kinds of particles into a pediatric antibiotic suspension.
3-12 Some people died in a hospital in Tehran under the usage of an imported general anesthetic for the wrong quality control process in the Central QC Laboratory of MoH.
3-13 Some imported blood preparations by a governmental department infected too many by HIV because of the poor QC methods employed by MoH.
3-14 A manufacturer sent seven files to MoH to gain production licenses. My comprehensive analysis proved that they were ABSOLUTELY, in the strongest meaning of the word, wrong and no one can find even a scientific or literal sentences in ALL of them. Many correspondences from MoH proved and yet proves that none of those huge and disastrous mistakes were detected by MoH officials or many pharmacist employees oh that company. Some of those drugs were Cardiac and anti-Asthmatic.
3-15 All bottles of a Pediatric dried suspension of Doxycycline released to market in spite of being degradated because of the high humidity of filling department.
3-16 Contaminated injectables (Oxytertracycline) with DUST of Carbon during the sealing step, released to market by the previous case company.
3-17 A hyperosmotic local anesthetic which was prepared by a governmental agent paralyzed some, especially from both legs following its injection into the spinal cord.
3-18 Washings and rain water entered the main water reservoir of a company for an unknown period of time in spite of repeated inspections of MoH agents and too many pseudo-pharmacist employees during in all those long years.
3-19 GMP is an antiproductive concept, for its exercising would stop everything. Instead manufacturers strictly obey BMP (Bad Manufacturing Process). Violation of any GMP rules, according to current regulations would lead a preparation to be recognized as rejected and in the light of this principles we are only able to produce rejected preparations.
4- On 29,09,2006 I entered Paris for an international exhibition on pharmaceutical materials. In hope of finding a solution for that crisis I stayed there but failed to gain any support to divulge this absolute case of Human Rights violation. In France I received tow negatives and after about twenty seven months decided to go back to Iran. In Vienna airport and after a short stop I experienced an intolerable anxiety and stress and lost my flight. In hope of finding a solution I applied in Austria but as in France I received tow negatives. By the rule of “No one can believe what he does not understand”, I asked in both countries my claims and documents be evaluated by experts but they disregarded this legal request.
5-During all of my professional life, somehow I was the best between my colleagues. All information and documents by help of them I discovered all those huge mistakes were also available to them but no one detected and noticed any mistakes. Successful and important improvements in nearly all aspect of pharmaceutical industry also include in my professional background. Opportunities for exercising habit of critical thinking and the exceptional capacity in application of creativity tied me strongly to my job in spite of depriving from all legitimate economical and social benefits. My collection of scientific books is more than three thousand volumes in different subjects including natural and human sciences. My studies in many aspect of English language are noticeable and are based on more than two hundred books on subjects like usual textbooks to linguistics and psychology of learning and teaching foreign languages. About sixty monolingual dictionaries in
different types and size and more than fifteen volumes on grammar at different levels are some subsets of my personal library. In Paris I studied three books on grammar two times and in more then three thousand pages. This language background and long and active experience in pharmaceutical industries make settlement a simple and short task at both social and professional levels. Considerable studies in Management, Organization, Organizational behavior, Ergonomy, Sociology, Social psychology, Psychology, Cognitive psychology, Educational and learning psychology, Philosophy and Philosophy of education provided me a nearly reliable mental awareness and critical mind.
3-THE followings are only a short list of those serious mistakes:
3-1 Usage delicate and unstable materials like vitamins five to seven years after the end of their Expiration Dates.
3-2 Huge mistakes in laboratory control methods of Raw Materials and finished products so that mistakes up to fifty percent, and usually more, could not be detected or could be introduced.
3-3 Mixing of raw well water with syrups for too many years because of a design defect in the filling machine.
3-4 correction of a totally wrong manufacturing procedure reduced the manufacturing time from ten hours in tow days to three hours in one day. A further correction of its formulation reduced its excipients about 1300 kg per 3000 l: this means their ignorance put the metabolic system of children under a severe pressure for absolutely no benefit or necessity. Its bitter taste and disgusting smell vanished for ever.
3-5 Defect in installation of a washing machine led to remaining about two milliliters of an extremely concentrated Chlorine water, one of the most dangerous Oxidizing agents, in the washed bottles used for bottling the above mentioned pediatric antibiotic suspension.
3-6 Usage an totally Inactive microbial preservative in an antacid suspension for too many years for the complete ignorance of the most basic principles of chemistry and biology.
3-7 For a while a company introduced a preparation without any Active component (drug molecules) into market for Economical reasons.
3-8 Active ingredient of an antacid suspension and tablets were respectively 25% and 16% less than the label amounts in at least two company.
3-9 In a comprehensive report, in more than one hundred pages, I proved that nearly what I knew till then in that company were wrong to the strongest and widest meaning of the word of wrong.
3-10 And there are too many other cases which I could not mention them for ,at least, the matter of space.
3-11 correction of filtering technique of a sugar syrup prevented the entrance of considerable amount of any kinds of particles into a pediatric antibiotic suspension.
3-12 Some people died in a hospital in Tehran under the usage of an imported general anesthetic for the wrong quality control process in the Central QC Laboratory of MoH.
3-13 Some imported blood preparations by a governmental department infected too many by HIV because of the poor QC methods employed by MoH.
3-14 A manufacturer sent seven files to MoH to gain production licenses. My comprehensive analysis proved that they were ABSOLUTELY, in the strongest meaning of the word, wrong and no one can find even a scientific or literal sentences in ALL of them. Many correspondences from MoH proved and yet proves that none of those huge and disastrous mistakes were detected by MoH officials or many pharmacist employees oh that company. Some of those drugs were Cardiac and anti-Asthmatic.
3-15 All bottles of a Pediatric dried suspension of Doxycycline released to market in spite of being degradated because of the high humidity of filling department.
3-16 Contaminated injectables (Oxytertracycline) with DUST of Carbon during the sealing step, released to market by the previous case company.
3-17 A hyperosmotic local anesthetic which was prepared by a governmental agent paralyzed some, especially from both legs following its injection into the spinal cord.
3-18 Washings and rain water entered the main water reservoir of a company for an unknown period of time in spite of repeated inspections of MoH agents and too many pseudo-pharmacist employees during in all those long years.
3-19 GMP is an antiproductive concept, for its exercising would stop everything. Instead manufacturers strictly obey BMP (Bad Manufacturing Process). Violation of any GMP rules, according to current regulations would lead a preparation to be recognized as rejected and in the light of this principles we are only able to produce rejected preparations.
4- On 29,09,2006 I entered Paris for an international exhibition on pharmaceutical materials. In hope of finding a solution for that crisis I stayed there but failed to gain any support to divulge this absolute case of Human Rights violation. In France I received tow negatives and after about twenty seven months decided to go back to Iran. In Vienna airport and after a short stop I experienced an intolerable anxiety and stress and lost my flight. In hope of finding a solution I applied in Austria but as in France I received tow negatives. By the rule of “No one can believe what he does not understand”, I asked in both countries my claims and documents be evaluated by experts but they disregarded this legal request.
5-During all of my professional life, somehow I was the best between my colleagues. All information and documents by help of them I discovered all those huge mistakes were also available to them but no one detected and noticed any mistakes. Successful and important improvements in nearly all aspect of pharmaceutical industry also include in my professional background. Opportunities for exercising habit of critical thinking and the exceptional capacity in application of creativity tied me strongly to my job in spite of depriving from all legitimate economical and social benefits. My collection of scientific books is more than three thousand volumes in different subjects including natural and human sciences. My studies in many aspect of English language are noticeable and are based on more than two hundred books on subjects like usual textbooks to linguistics and psychology of learning and teaching foreign languages. About sixty monolingual dictionaries in
different types and size and more than fifteen volumes on grammar at different levels are some subsets of my personal library. In Paris I studied three books on grammar two times and in more then three thousand pages. This language background and long and active experience in pharmaceutical industries make settlement a simple and short task at both social and professional levels. Considerable studies in Management, Organization, Organizational behavior, Ergonomy, Sociology, Social psychology, Psychology, Cognitive psychology, Educational and learning psychology, Philosophy and Philosophy of education provided me a nearly reliable mental awareness and critical mind.
6- I like to bring this letter to its end by some quotations from Mill whose wisdom and
humanity glazes eyes of the wise and no one ignores him without a great
loss of knowledge and discoveries on nature of Human and Power as a
necessary and unavoidable Evil of his life in societies:
Whatever precautions might be taken against the oppressive exercise of power (page?, On Liberty.)
CV
MOHAMMAD POUR, BAGHER(PHARM. D.)
NO 32, BARZEGARPOUR LANE,
HKOSH ST.,
MORTAZAVI CROSS,
TEHRAN 13547,
IRAN.bmp1337@yahoo.com
PERSONAL DETAILS:
FAMILY NAME: MOHAMMAD POUR
NAME: BAGHER
DOB: 30/04/1958
POB: TEHRAN/IRAN
NO OF ID CARD: 2047
FATHER: MOHAMMAD HOSSEIN
MARRAGE: DIVORCED
CHILDREN: MOHAMMAD; 20 YEARS OLD; TEHRAN/IRAN; UNIVERSITY STUDENT OF PHYSICS IN TEHRAN.
EDUCATION:
1-HIGHSCHOOL DIPLOMA: 1976, NATURAL SCIENCES
2-UNIVERSITY DIPLOMA: PHARM. D.; TABRIZ UNIVERSITY, TABRIZ, IRAN; 1976-1985 (INCLUDING REVOLUTION & CULTURAL REVOLUTION OFF-DAYS)
3-OTHERS: ISO 9000 SERIES, TWO COURSES: 1-STRUCTURE & DEVELOPMENT, 2-QUALITY MANAGEMENT AUDITOR.
PROFFESSIONAL BACKGROUND:
1-APR 1985-JUL 1986; RAZAK PHARMA CO, MANAGER OF PACKING DEPT.
2-JUL 1986-NOV 1988; EMERGENCY MILLITARY SERVICE.
3-MAR 1986-NOV 1990; MANDATORY SERVICE FOR MOH.
4-JAN 1991-AUG 1992; ALBORZ DAROU PHARM CO, MANAGER OF LIQUID DEPT.
5-JAN 1993-OCT 1994; PHARMA CHIMIE; R&D DEPT. MANAGER.
6-OCT 1994-SEP 1995; PYRAIEH COSMETIC & HYGIENIC CO; RESPONSIBLE PHARMACIST.
7-DEC 1995-JAN 1997; LOGHMAN PHARM CO; PRODUCTION MANAGER.
8-NOV 1997-VOV 1999; ALHAVI PHARM CO; PRO- DUCTION MANAGER.
9-JUN 2000-JUN 2001; TEHRAN DAROU PHARM CO;
RESPONSIBLE PHARMACIST.
10-SEP 2002-DEC 2006; SHAHRE DAROU PHARM CO;
LIQUID PRODUCTION MANAGER; the last position:
QC MANGAER for more than three years.
ACHIEVEMENTS:
A NECESSARY INTRODUCTION: Because of my special interests in nearly all aspect of pharmaceutical production, always I was involved in many different kind of professional and scientific activities. At the same moment there were two others reason for the diversity of my interests and engagement in different aspect of pharmaceutical production. The first reason is that any kind of industrial production is an integrated chain and steps of different activities that form, or MUST form a logical sequence of tasks in each, the previous step object is the initial material for the next: thus the successful result or end of each step MUST be evaluated on, first, the quality of initial material (as defined above) and, second, the correctness of the next step activity AND its proper and successful exercise. So, under the light of the mentioned principle, I was always aware that detection of the nature of each single activity OR problem depends totally and absolutely
on our understanding of all the production procedure as a Single and Unified Activity, and secondly without having a clear mental map and theoretical understanding of what WE are doing, neither we could evaluate the correctness of each step achievement nor we would be able to Detect, Define, and solve our problems. This was the first reason of my notice to and interest in different fields of pharmaceutical production from QC of materials to Formulation and Process Design up to the definitions of quality parameters and the methods of their assessment.
And on the basis of my understanding and familiarity with the educational deficiencies in universities, and more importantly, the gross dependence and reliance of Pharmaceutical industry as a branch of Chemical Industry on Natural Sciences, I have tried to compensate what educational system was never able to provide, AND KNOWING THAT without a basic understanding of them nothing could be done without a gross inclusion of errors and fatal mistakes, I tried, as far as I could, to Absorb what I needed as an Industrial pharmacist, what usually none of my colleagues could provide me as a pharmacist and colleague. For example, my first official position as QC manager was in Shahre Darou but I was the main participant of QC lab in Alhavi or in Alborz Darou, and as the manager of Production my engagement in understanding all possible scientific or technical basis of our activity was clear, deep, and firm. This can be believed noticing the diversity of my
activities and corrections which spread from too early initial step of Water System up to designing and writing the most com-prehensive and practical and Scientific based Analytical Procedure FOR QC Laboratory and up to Stability and Organoleptic properties of medicinals. Two principles have always guided my professional life, from biology and manage- ment: Nature Does Nothing for Nothing (We need have reasons for our choices) & Always There Could Be a Better Way (We must keep our mind open to new ideas and to the future). Therefore all the below cases are the fruits of one or both of the above Principles.
Here I could not provide a complete list of my activities nor I could provide necessary convincing information on them. This list only mentions the core and heart of the problems without necessarily any notice to the company and some time out of historical order and under the force of limited time. (a late contemporary Iranian poet says: And suddenly/ Very soon/ It becomes late; Ghaisar-e Amin Pour.)
A SHORT LIST OF ACHIEVEMENTS
1)Correction of many mistakes in different laboratory control methods of Raw Materials and finished products in many companies; mistakes up to fifty percent, and usually more, could not be detected or could be introduced.
2)Mixing of raw well water with syrups after too many years prevented and it was because of a design defect in the filling machine.
3)Correction of a totally wrong manufacturing procedure reduced the manufacturing time of a pediatric liquid antibiotic from ten hours in tow days to three hours in one day and consequently production capacity of that production increased 600%. A further correction of its formulation reduced its excipients about 1300 kg per 3000 Liter (And scientific proof for the former procedure being mistake and justification of correctness of the new were totally based on the best texts of the time.) Its bitter taste and disgusting smell and taste and permanent default of undispessed agglomerates vanished for ever.
4)Defect in installation of a washing machine led to remaining about two milliliters of an extremely concentrated Chlorine water in the washed bottles used for bottling the above mentioned pediatric antibiotic suspension.
5)Usage an totally Inactive microbial preservative in an antacid suspension corrected after too many years and by the aid of the most basic principles of chemistry and biology an active one selected.
6)Active ingredients of an antacid suspension and tablets were respectively 25% and 16% less than the label amounts in at least two company and for an unknown time; I corrected them.
7)In a comprehensive report, in more than one hundred pages, I proved that nearly what I knew till then in that company were wrong to the strongest and widest meaning of the word of wrong and provided detailed comments on all of them in three field: Production, QC, and Management.
8)Correction of filtering technique of a sugar syrup prevented the entrance of a considerable amount of any kinds of particles into a pediatric antibiotic suspension.
9)My comprehensive analysis (in about two hundred pages), as the Responsible Pharmacist, of seven files on design, production, and QC procedures of six important medicines (some were life-saving) proved that they were ABSOLUTLY wrong in the strongest meaning of the word.
10)Correction of design of entrance of the main water reservoir of a company prevented entrance of washings and rain water in it and it continued for an unknown period of time
11)Correction of an administrative procedure reduced the usage of plastic spoons and aluminum caps up to 25%.
12) Correction of water purifying system where the saline water for regeneration of ion-exchanging resins was prepared in old and oxidized iron container and was dark-brown by plentifullnes of Ferric Oxide.
13)Granulating procedure of an antibiotic tablet was totally unjustified and wrong so dried granules were completely incompressible and pressing were divided into many small time-consuming and hard steps and finally lead to extremely fragile and rough surface tablets.
14)Application the simplest rules of Algebra and Arithmetic proved that nearly all QC calculations are wrong and interpretation of results were arbitrary and had no scientific basis or support in the eyes of International Authorities like FDA and...
15)As a responsible person in a hygienic company I did a vast investigation on formulation of Dishwashing Liquids and to a great extent discovered none knew the exact scientific basis of making a chemically (at least) justified product and usually the mixing order of components were wrong so unwanted chemical reaction between those that had not to bear it, lead to destruction of chemicals and a production of unknown components with unpredictable
activity and side effects. That article is available.
16)Correction of preparation method of a cellulosic gum increased its viscosity 300% and reduced its usage to one-third.
17)Investigation of spectroscopic method of analysis in USP proved that it was (and ‘is’ till today) incomplete and BP provided no method; even the USP method requires you the answer to be able to solve your problem!! I find a very simple and extremely useful formula to complete USP method and removed its logical controversy. Further examination of that formula showed that it can be used successfully in designing in-home methods of spec- troscopic measurements and make us able to do what we want by positive application of our limitations and possibilities. The reply of the Chief Editor of that part of USP was the strangest possible by a USP’s Editor:
We do not have time to study your formula and letter.
18)In reply to request of a General Manager I wrote a detailed report on nearly all aspect of the life of that organization. In that letter I proved scientific mistakes had invaded all era of Organizational Life and quality is Accidental and Unintentional. That letter contains about fifty comments on all aspects, directly or indirectly, quality both as an activity or a goal and, the importance of production as the heart of an industrial unit. In another activity I corrected the analytical methods of the following materials with the stated percentage of errors:
MgO, minus 40%; Fe Fum., plus 900%; assay test of a Decongestant in a syrup, minus 92.5 in one respect and plus 1250% in another; Ca(ion) in a capsule minus 100%. And too many others, for example wrong adjustment of a Colloid Mill lead to destruction of about 200,000 bottles of Chloramphenicol suspension.
19)Stabilization of an extremely unstable Ferrous solution in a new formulation and reducing its Coloring effect on teeth.
20)Designing and improving many technical forms of production, QC laboratory, and administrative department by: Application of similarity in similar forms; Canceling unrelated information and/or items; Inclusion of necessities; and Finally adaptation of their design and follow with the administrative procedures and require- ments of GMP, ISO, and Internal Design of organization. Importance of this principle has made it a feature and criteria of suitability of organizations by this formula:
Structure and efficiency of a well-designed organization,
And the competence of its creators ,
are defined in, and mirrored by its FORMS respectively.
(in other words: good FORMS are self-defining and the best guidance and MAP on your location in the organization.) Many forms by application of this principle were corrected.
21)Application of ‘USP Introduction’s recommendation, or what can be even interpreted as ORDER ,on the Necessity of Internalizing and Absorption of scientific basis of each test and monograph, proved that by simple translation of them into the mother-tongue of technicians and rewriting or typing them in a tidy format nearly Nothing of knowledge would be gained and no responsibility would be fulfilled, and brings not even a small portion of practical efficiency and expert: Any activity in the filed of application of Natural Sciences, in their most modern meaning of them, without bearing a Good and Deep understanding of their theoretical ground in mind, is Only and Only a ‘sleepwalking’ and sleepwalker fells and stops very soon by the first obstacle.
Some sample were done. All the above huge mistakes in analytical procedures and results were the fruits of ignorance to that order and its importance and were solved only ay its application. Those samples proved that in some cases the Supporting Information of an analysis could be up to ten times of its text and need a lot of references be used at the same time.
MORE POINTS ON PERSONAL INTERESTS:
1)My personal library has about three thousand volumes of books. They could be divided into two main category; some on Human sciences and second those on Natural sciences. Some books in the former part have some applications on organizations and by this way find some links to environmental parameters of human society; for example principles of philosophy, psychology, sociology, management or even politics and some concepts of biology have strong applications in organizations and through this way could help in understanding of those specific problems which have been a constant part of human life in society and history.
2)My Natural Sciences books are on the subjects: Physics (as the king, head and spring of all other discipline in this field), Calculus, Linear Algebra, Geometry, Statistics, Pharmaceutical statistics, Statistical design, Thermodynamic, General chemistry, Organic chemistry, Inorganic chemistry, Medicinal chemistry, Pharmaceutical chemistry, Physical chemistry, Instrumental analytical chemistry, Unit operations in chemical engineering, Perry’s handbook of chemical engineering, Engineering and mechanical design, Industrial pharmacy(many), Pharmacology: Basic, Clinical, Molecular; Drug information, Internal medicine, Biopharmaceutics, Pharmacokinetics, Quality control, Statistical quality control, GMP regulations, and …
3)My Human sciences books on related fields to Organizations are on subjects: Sociology, Psychology, Social psychology, Management, Organizational Behavior,
Organization design, Ergonomy, Job design, ISO applications and …
4)My main interest is reading and reading and reading, and then Hiking, Photography, Handicraft, Persian Poem and Language and Vocabulary and Prose style; English language (more than two hundred books on different aspect of English language including about sixty volume monolingual English-English dictionaries of different kinds and size and publishers).
5)This letter is the example of my writing ability in English and, my speaking is nearly at the same level and I have no difficulty in reading, understanding and interpretation of scientific and pharmaceutical texts and references.
B Mohammad pour
Pharm. D.
May 2009.
NO 32, BARZEGARPOUR LANE,
HKOSH ST.,
MORTAZAVI CROSS,
TEHRAN 13547,
IRAN.bmp1337@yahoo.com
PERSONAL DETAILS:
FAMILY NAME: MOHAMMAD POUR
NAME: BAGHER
DOB: 30/04/1958
POB: TEHRAN/IRAN
NO OF ID CARD: 2047
FATHER: MOHAMMAD HOSSEIN
MARRAGE: DIVORCED
CHILDREN: MOHAMMAD; 20 YEARS OLD; TEHRAN/IRAN; UNIVERSITY STUDENT OF PHYSICS IN TEHRAN.
EDUCATION:
1-HIGHSCHOOL DIPLOMA: 1976, NATURAL SCIENCES
2-UNIVERSITY DIPLOMA: PHARM. D.; TABRIZ UNIVERSITY, TABRIZ, IRAN; 1976-1985 (INCLUDING REVOLUTION & CULTURAL REVOLUTION OFF-DAYS)
3-OTHERS: ISO 9000 SERIES, TWO COURSES: 1-STRUCTURE & DEVELOPMENT, 2-QUALITY MANAGEMENT AUDITOR.
PROFFESSIONAL BACKGROUND:
1-APR 1985-JUL 1986; RAZAK PHARMA CO, MANAGER OF PACKING DEPT.
2-JUL 1986-NOV 1988; EMERGENCY MILLITARY SERVICE.
3-MAR 1986-NOV 1990; MANDATORY SERVICE FOR MOH.
4-JAN 1991-AUG 1992; ALBORZ DAROU PHARM CO, MANAGER OF LIQUID DEPT.
5-JAN 1993-OCT 1994; PHARMA CHIMIE; R&D DEPT. MANAGER.
6-OCT 1994-SEP 1995; PYRAIEH COSMETIC & HYGIENIC CO; RESPONSIBLE PHARMACIST.
7-DEC 1995-JAN 1997; LOGHMAN PHARM CO; PRODUCTION MANAGER.
8-NOV 1997-VOV 1999; ALHAVI PHARM CO; PRO- DUCTION MANAGER.
9-JUN 2000-JUN 2001; TEHRAN DAROU PHARM CO;
RESPONSIBLE PHARMACIST.
10-SEP 2002-DEC 2006; SHAHRE DAROU PHARM CO;
LIQUID PRODUCTION MANAGER; the last position:
QC MANGAER for more than three years.
ACHIEVEMENTS:
A NECESSARY INTRODUCTION: Because of my special interests in nearly all aspect of pharmaceutical production, always I was involved in many different kind of professional and scientific activities. At the same moment there were two others reason for the diversity of my interests and engagement in different aspect of pharmaceutical production. The first reason is that any kind of industrial production is an integrated chain and steps of different activities that form, or MUST form a logical sequence of tasks in each, the previous step object is the initial material for the next: thus the successful result or end of each step MUST be evaluated on, first, the quality of initial material (as defined above) and, second, the correctness of the next step activity AND its proper and successful exercise. So, under the light of the mentioned principle, I was always aware that detection of the nature of each single activity OR problem depends totally and absolutely
on our understanding of all the production procedure as a Single and Unified Activity, and secondly without having a clear mental map and theoretical understanding of what WE are doing, neither we could evaluate the correctness of each step achievement nor we would be able to Detect, Define, and solve our problems. This was the first reason of my notice to and interest in different fields of pharmaceutical production from QC of materials to Formulation and Process Design up to the definitions of quality parameters and the methods of their assessment.
And on the basis of my understanding and familiarity with the educational deficiencies in universities, and more importantly, the gross dependence and reliance of Pharmaceutical industry as a branch of Chemical Industry on Natural Sciences, I have tried to compensate what educational system was never able to provide, AND KNOWING THAT without a basic understanding of them nothing could be done without a gross inclusion of errors and fatal mistakes, I tried, as far as I could, to Absorb what I needed as an Industrial pharmacist, what usually none of my colleagues could provide me as a pharmacist and colleague. For example, my first official position as QC manager was in Shahre Darou but I was the main participant of QC lab in Alhavi or in Alborz Darou, and as the manager of Production my engagement in understanding all possible scientific or technical basis of our activity was clear, deep, and firm. This can be believed noticing the diversity of my
activities and corrections which spread from too early initial step of Water System up to designing and writing the most com-prehensive and practical and Scientific based Analytical Procedure FOR QC Laboratory and up to Stability and Organoleptic properties of medicinals. Two principles have always guided my professional life, from biology and manage- ment: Nature Does Nothing for Nothing (We need have reasons for our choices) & Always There Could Be a Better Way (We must keep our mind open to new ideas and to the future). Therefore all the below cases are the fruits of one or both of the above Principles.
Here I could not provide a complete list of my activities nor I could provide necessary convincing information on them. This list only mentions the core and heart of the problems without necessarily any notice to the company and some time out of historical order and under the force of limited time. (a late contemporary Iranian poet says: And suddenly/ Very soon/ It becomes late; Ghaisar-e Amin Pour.)
A SHORT LIST OF ACHIEVEMENTS
1)Correction of many mistakes in different laboratory control methods of Raw Materials and finished products in many companies; mistakes up to fifty percent, and usually more, could not be detected or could be introduced.
2)Mixing of raw well water with syrups after too many years prevented and it was because of a design defect in the filling machine.
3)Correction of a totally wrong manufacturing procedure reduced the manufacturing time of a pediatric liquid antibiotic from ten hours in tow days to three hours in one day and consequently production capacity of that production increased 600%. A further correction of its formulation reduced its excipients about 1300 kg per 3000 Liter (And scientific proof for the former procedure being mistake and justification of correctness of the new were totally based on the best texts of the time.) Its bitter taste and disgusting smell and taste and permanent default of undispessed agglomerates vanished for ever.
4)Defect in installation of a washing machine led to remaining about two milliliters of an extremely concentrated Chlorine water in the washed bottles used for bottling the above mentioned pediatric antibiotic suspension.
5)Usage an totally Inactive microbial preservative in an antacid suspension corrected after too many years and by the aid of the most basic principles of chemistry and biology an active one selected.
6)Active ingredients of an antacid suspension and tablets were respectively 25% and 16% less than the label amounts in at least two company and for an unknown time; I corrected them.
7)In a comprehensive report, in more than one hundred pages, I proved that nearly what I knew till then in that company were wrong to the strongest and widest meaning of the word of wrong and provided detailed comments on all of them in three field: Production, QC, and Management.
8)Correction of filtering technique of a sugar syrup prevented the entrance of a considerable amount of any kinds of particles into a pediatric antibiotic suspension.
9)My comprehensive analysis (in about two hundred pages), as the Responsible Pharmacist, of seven files on design, production, and QC procedures of six important medicines (some were life-saving) proved that they were ABSOLUTLY wrong in the strongest meaning of the word.
10)Correction of design of entrance of the main water reservoir of a company prevented entrance of washings and rain water in it and it continued for an unknown period of time
11)Correction of an administrative procedure reduced the usage of plastic spoons and aluminum caps up to 25%.
12) Correction of water purifying system where the saline water for regeneration of ion-exchanging resins was prepared in old and oxidized iron container and was dark-brown by plentifullnes of Ferric Oxide.
13)Granulating procedure of an antibiotic tablet was totally unjustified and wrong so dried granules were completely incompressible and pressing were divided into many small time-consuming and hard steps and finally lead to extremely fragile and rough surface tablets.
14)Application the simplest rules of Algebra and Arithmetic proved that nearly all QC calculations are wrong and interpretation of results were arbitrary and had no scientific basis or support in the eyes of International Authorities like FDA and...
15)As a responsible person in a hygienic company I did a vast investigation on formulation of Dishwashing Liquids and to a great extent discovered none knew the exact scientific basis of making a chemically (at least) justified product and usually the mixing order of components were wrong so unwanted chemical reaction between those that had not to bear it, lead to destruction of chemicals and a production of unknown components with unpredictable
activity and side effects. That article is available.
16)Correction of preparation method of a cellulosic gum increased its viscosity 300% and reduced its usage to one-third.
17)Investigation of spectroscopic method of analysis in USP proved that it was (and ‘is’ till today) incomplete and BP provided no method; even the USP method requires you the answer to be able to solve your problem!! I find a very simple and extremely useful formula to complete USP method and removed its logical controversy. Further examination of that formula showed that it can be used successfully in designing in-home methods of spec- troscopic measurements and make us able to do what we want by positive application of our limitations and possibilities. The reply of the Chief Editor of that part of USP was the strangest possible by a USP’s Editor:
We do not have time to study your formula and letter.
18)In reply to request of a General Manager I wrote a detailed report on nearly all aspect of the life of that organization. In that letter I proved scientific mistakes had invaded all era of Organizational Life and quality is Accidental and Unintentional. That letter contains about fifty comments on all aspects, directly or indirectly, quality both as an activity or a goal and, the importance of production as the heart of an industrial unit. In another activity I corrected the analytical methods of the following materials with the stated percentage of errors:
MgO, minus 40%; Fe Fum., plus 900%; assay test of a Decongestant in a syrup, minus 92.5 in one respect and plus 1250% in another; Ca(ion) in a capsule minus 100%. And too many others, for example wrong adjustment of a Colloid Mill lead to destruction of about 200,000 bottles of Chloramphenicol suspension.
19)Stabilization of an extremely unstable Ferrous solution in a new formulation and reducing its Coloring effect on teeth.
20)Designing and improving many technical forms of production, QC laboratory, and administrative department by: Application of similarity in similar forms; Canceling unrelated information and/or items; Inclusion of necessities; and Finally adaptation of their design and follow with the administrative procedures and require- ments of GMP, ISO, and Internal Design of organization. Importance of this principle has made it a feature and criteria of suitability of organizations by this formula:
Structure and efficiency of a well-designed organization,
And the competence of its creators ,
are defined in, and mirrored by its FORMS respectively.
(in other words: good FORMS are self-defining and the best guidance and MAP on your location in the organization.) Many forms by application of this principle were corrected.
21)Application of ‘USP Introduction’s recommendation, or what can be even interpreted as ORDER ,on the Necessity of Internalizing and Absorption of scientific basis of each test and monograph, proved that by simple translation of them into the mother-tongue of technicians and rewriting or typing them in a tidy format nearly Nothing of knowledge would be gained and no responsibility would be fulfilled, and brings not even a small portion of practical efficiency and expert: Any activity in the filed of application of Natural Sciences, in their most modern meaning of them, without bearing a Good and Deep understanding of their theoretical ground in mind, is Only and Only a ‘sleepwalking’ and sleepwalker fells and stops very soon by the first obstacle.
Some sample were done. All the above huge mistakes in analytical procedures and results were the fruits of ignorance to that order and its importance and were solved only ay its application. Those samples proved that in some cases the Supporting Information of an analysis could be up to ten times of its text and need a lot of references be used at the same time.
MORE POINTS ON PERSONAL INTERESTS:
1)My personal library has about three thousand volumes of books. They could be divided into two main category; some on Human sciences and second those on Natural sciences. Some books in the former part have some applications on organizations and by this way find some links to environmental parameters of human society; for example principles of philosophy, psychology, sociology, management or even politics and some concepts of biology have strong applications in organizations and through this way could help in understanding of those specific problems which have been a constant part of human life in society and history.
2)My Natural Sciences books are on the subjects: Physics (as the king, head and spring of all other discipline in this field), Calculus, Linear Algebra, Geometry, Statistics, Pharmaceutical statistics, Statistical design, Thermodynamic, General chemistry, Organic chemistry, Inorganic chemistry, Medicinal chemistry, Pharmaceutical chemistry, Physical chemistry, Instrumental analytical chemistry, Unit operations in chemical engineering, Perry’s handbook of chemical engineering, Engineering and mechanical design, Industrial pharmacy(many), Pharmacology: Basic, Clinical, Molecular; Drug information, Internal medicine, Biopharmaceutics, Pharmacokinetics, Quality control, Statistical quality control, GMP regulations, and …
3)My Human sciences books on related fields to Organizations are on subjects: Sociology, Psychology, Social psychology, Management, Organizational Behavior,
Organization design, Ergonomy, Job design, ISO applications and …
4)My main interest is reading and reading and reading, and then Hiking, Photography, Handicraft, Persian Poem and Language and Vocabulary and Prose style; English language (more than two hundred books on different aspect of English language including about sixty volume monolingual English-English dictionaries of different kinds and size and publishers).
5)This letter is the example of my writing ability in English and, my speaking is nearly at the same level and I have no difficulty in reading, understanding and interpretation of scientific and pharmaceutical texts and references.
B Mohammad pour
Pharm. D.
May 2009.
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