On Thursday, June 18, 2009 5:19 PM, bagher mohammadpour
<bmp1337@yahoo.com> wrote to enquiry@dfid.gov.uk
<enquiry@dfid.gov.uk>;:
A person may cause evil to others
not only by his actions
but by his INACTION,
and in either case he is justly
accountable to them for INJURY.
(page 70)
Very few facts
are able to tell their story
without comments
to bring out their meaning.
(page 80)
John Stuart Mill, On Liberty,
1859, in Penguin Classics 1985
When the foundations are being destroyed,
what can the righteous do?
(Psalm 11:3)
IN IRAN
the struggle between Liberty and Authority
has never been so harsh and bloody
during the last century.
The government uses all his power
against his subjects
no less than against external enemies.
Mill says
“But in political and philosophical theories
success disclose defaults and infirmities
which failure might have concealed from observation.”
So the severity of this struggle
puts a further proof on
the Tyrannical nature of ideological and theological
(as happened in Europe) regimes.
B. Mohammad pour,
Paris, France.bmp1337@yahoo.com
The Right honorable Gordon Brown
The Prime minister of England
Today it is an received opinion and belief, both nationally and internationally, that: Any commitment to advancement of Human Rights in Iran must be asserted by deeds, for words, on this subject, it is a long time, have nearly exhausted their POWER.
What I am writing you about is an absolutely incredible case of HRs violation in the history of the Islamic Government and the worst of them. If only critics and social activists and political and journalists figures are subject to political and judicial persecution and torture, this crisis affects all innocent members of a whole nation and no one could escape from its dangers. The simplest cases of those mistakes deserve up to few million dollars of fine and about ten years jail in the U.S.A and Europe. If violation on human rights in Iran, like in all other countries, is measured according to the current international and accepted understanding of the subject, I assure you what I try to divulge is the worst case in the world of a deliberate and nationwide violation has ever been committed by any government against its people. My claims are totally based on too many official documents from many manufacturers and the Ministry of Health and they prove
that this problem is a STRUCTURAL defect and has no simple and easy solution; no expert could believe what is going on in Iran in this field.
I and my people are in Urgent need of a minute part of international humanitarian aids of your country as a serious critics of the Islamic Government for his tyrannical and inhumane deeds and behavior. Spending more than thirty months in Europe has depleted all my financial supports. My long experience in pharmaceutical industries and abilities in English language (more information in the enclosed letter) make my settlement an easy and successful task and here I promise to pay back the cost of my reaching your country.
I hope your humane interests and commitment of your country to advancement of HRs help me urgently to bring this 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 social life during the last century.
So my request for support and being in your country is not a kind of ordinary immigration request which are normally subject of along and time-consuming procedure; it is somehow a political and national one that requires your special favor and supports. I hope receive your supports very soon till all the Iranians benefit from the righteous commitment of your country to their well-being.
In blue colour, bellow, is my letter to MHRA. Without their assessment
and evaluation all the truth will miss because according to J. S. Mill:
Very few facts
are able to tell their story
without comments
to bring out their meaning.
Respectfully yours
B Mohammad pour
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 DISASTEROUS 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:
§- Usage delicate and unstable materials like vitamins five to seven years after the end of their Expiration Dates.
§- 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.
§- Mixing of raw well water with syrups for too many years because of a design defect in the filling machine.
§- 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.
§- 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.
§- 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.
§- For a while a company introduced a preparation without any Active component (drug molecules) into market for Economical reasons.
§- Active ingredient of an antacid suspension and tablets were respectively 25% and 16% less than the label amounts in at least two company.
§- 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.
§- correction of filtering technique of a sugar syrup prevented the entrance of considerable amount of any kinds of particles into a pediatric antibiotic suspension.
§- 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.
§- Some imported blood preparations by a governmental department infected too many by HIV because of the poor QC methods employed by MoH.
§- A manufacturer sent seven files to MoH to gain production licenses. My comprehensive analysis proved that they were ABSOLUTLY, 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.
§- All bottles of a Pediatric dried suspension of Doxycycline released to market in spite of being degraded because of the high humidity of filling department.
§- Contaminated injectables (Oxytertracycline) with DUST of Carbon during the sealing step, released to market by the previous case company.
§- A hyperosmotic local anesthetic which was prepared by a governmental agent paralyzed some, especially from both legs following its injection into the spinal cord.
§- 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.
§- GMP is an anti-productive 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 in 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 even one of those huge 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.
My DISASTEROUS 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:
§- Usage delicate and unstable materials like vitamins five to seven years after the end of their Expiration Dates.
§- 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.
§- Mixing of raw well water with syrups for too many years because of a design defect in the filling machine.
§- 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.
§- 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.
§- 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.
§- For a while a company introduced a preparation without any Active component (drug molecules) into market for Economical reasons.
§- Active ingredient of an antacid suspension and tablets were respectively 25% and 16% less than the label amounts in at least two company.
§- 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.
§- correction of filtering technique of a sugar syrup prevented the entrance of considerable amount of any kinds of particles into a pediatric antibiotic suspension.
§- 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.
§- Some imported blood preparations by a governmental department infected too many by HIV because of the poor QC methods employed by MoH.
§- A manufacturer sent seven files to MoH to gain production licenses. My comprehensive analysis proved that they were ABSOLUTLY, 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.
§- All bottles of a Pediatric dried suspension of Doxycycline released to market in spite of being degraded because of the high humidity of filling department.
§- Contaminated injectables (Oxytertracycline) with DUST of Carbon during the sealing step, released to market by the previous case company.
§- A hyperosmotic local anesthetic which was prepared by a governmental agent paralyzed some, especially from both legs following its injection into the spinal cord.
§- 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.
§- GMP is an anti-productive 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 in 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 even one of those huge 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.
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.
Usually there are persons
who form an exception
to the apparent unanimity of the world on any subject… and truth would lose something
by their silence
(On Liberty, page 111).
The mere refusal to bend the knee
to the customs and power
is itself a service
(On Liberty, page 130).
Whatever precautions
might be taken against
the oppressive exercise of power
(On Liberty, page?)
might be taken against
the oppressive exercise of power
(On Liberty, page?)
E P I L O G U E
Regarding current legal system and scientific status of pharmaceutical industries in the modern world, I strongly believe that divulging the crisis in the pharmaceutical industries of IRAN would discover a new and incredible dimension of dark and brutal nature of the Islamic government and would have its vital and devastating consequences in practical criticism of theological and ideological types of governments and, at the same time will be the biggest defense in favor of Iranians against the tyrannical application power of Islamic regime.
&&&&&&&&
And at the personal level I hope your and your Country’s support provide me the opportunity of life in an Open, Democratic and Modern society after a long struggle with a wild Authority in the most hidden and darkest border of fight.
&&&&&&&&
Before the announcement of History enslaving the soul and sprit of mankind irreversible in Iran, we have duty and responsibility to do anything possible to stop it for ever; for human is deserved to be the subject only of his Will’s power. (inspired by Mill)
On Thursday, June 25, 2009 5:27 PM, MHRA Information Centre wrote:
Dear Mr B Mohammad pour,
Manufacturing
sites in the UK and sites in countries that manufacture product for the
UK are regularly inspected to ensure compliance
to the
EU Good Manufacturing Practic Guidelines (GMP). If a site fails to meet
applicable GMP standard then their license to manufacture
pharmaceuticals can be varied or revoked.
If
a site continues to manufacture (ie manufactures without a license and
hence illegally) then Enforcement powers exist such that individuals in
the UK can be prosecuted under the Medicines Act.
The penalties applicable in such casesare:
2 years imprisonment and/or unlimited* fine.
We can not comment on what should or does happens in non EU countries if Good Manufacturing Practice is not adhered to.
Your sincerely
BJ Wright Group Manager Inspection
Medicines and Healthcare products Regulatory Agency
Tel: 020 7084 2000
Tel: 020 7084 2000
*For the limit of "unlimited" click on
___________________________________________________________________________________________
From:bagher mohammadpour [mailto:bmp1337@yahoo.com]
Sent:02 June 2009 12:56
To:MHRA Information Centre
Subject:Fw: An Incredable Report From....a little pharmacist
Sent:02 June 2009 12:56
To:MHRA Information Centre
Subject:Fw: An Incredable Report From....a little pharmacist
----- Forwarded Message ----
From:Legal and Ethical Advisory Service
To:bmp1337@yahoo.com
Sent:Monday, June 1, 2009 5:23:14 PM
Subject:FW: An Incredable Report From....a little pharmacist
_________________________________________________
From:Legal and Ethical Advisory Service
To:bmp1337@yahoo.com
Sent:Monday, June 1, 2009 5:23:14 PM
Subject:FW: An Incredable Report From....a little pharmacist
_________________________________________________
Dear Madam /Sir
I am an Iranian pharmacist with more than 20 years of experience in the pharmaceutical industries of Iran.
The following list is not a sample, it shows the NATURE of nearly all activities which are needed to be done in a typical pharmaceutical company to be a pharmaceutical company, in nearly all domestic manufacturers of medicinals. As a colleague of you from a remote country, I like to know professional, scientific, and legal assessment and evaluation of Pharmacy, as an established international discipline, on them and that National System (including Ministry of Health) which supports them. You do not need here to hear more and again why no one dares to speak of this kind of problems in Iran . What would be the consequences of such mistakes in Europe or the North America , according to current law and regulations for such manufactures and officials?
§- Usage delicate and unstable materials like vitamins five to seven years after the end of their Expiration Dates. (COMPANY: Alhavy Co.; Tehran)
§- 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. (COMPANY: Alhavy Co., Tehran)
§- Mixing of raw well water with syrups for too many years because of a design defect in the filling machine. (COMPANY: Alborz Daru; Qazvin)
§- 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. 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. (COMPANY: Alborz Daru; Qazvin)
§- For a while a company introduced a preparation without any Active component (drug molecules) into market for Economical reasons. (According to a Respector of MOH)
§- Active ingredient of an antacid suspension and tablets were respectively 25% and 16% less than the label
amounts in at least two companies. (COMPANY: Alborz Daru; Qazvin)
§- 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. (COMPANY: Alhavi; Tehran)
§- correction of filtering technique of a sugar syrup prevented the entrance of considerable amount of any kinds of particles into a pediatric antibiotic suspension. (COMPANY: Alborz Daru; Qazvin)
§- 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.
§- Some imported blood preparations by a governmental department infected too many by HIV because of the poor QC methods employed by MoH.
§- A manufacturer sent seven files to MoH to gain production licenses. My comprehensive analysis proved that they were ABSOLUTLY, 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. (COMPANY: Tehran Daru; Tehran)
§- 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. (COMPANY: Razak; Tehran)
§- Contaminated injectables (Oxytertracycline) with DUST of Carbon during the sealing step, released to market by the previous case company. (COMPANY: Razak; Tehran)
§- A hyperosmotic local anesthetic which was prepared by a governmental agent paralyzed some, especially from both legs following its injection into the spinal cord.
§- 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. (COMPANY: Tehran Daru; Tehran)
§- 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.
I believe that you mention this letter and its content Strictly confidential and professional as your reply would be considered so.
Thank you for your attention, time and kindness. I am eagerly looking forward to hear from you as soon as possible. Your favor would not be forgotten and I am in need of your guidance.
Faithfully your
B Mohammad pour,
Pharm. D.
B Mohammad pour,
Pharm. D.
______________________________________________________________________
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