Dear Pharmacist,
If you are planning to move abroad as a Pharmacist, just Follow link and get important information about Requirement, Registration & eligibility criteria.
http://www.fip.org/files/fip/HR/final%20report/latest/appendix%206.PDF
Wednesday, September 21, 2011
Saturday, September 3, 2011
Why Should Prefer Generic ?
The Generic advantage
This flyer has been designed to provide you with important and accurate information
about generic drugs and their use. Please consider the option generics provide for those who want to receive high quality medications at considerably lower prices. Once you decide generics may be the right choice for you, please discuss with your physician or pharmacist the possibility of receiving equivalent generic medications for your prescriptions. Bear in mind that nearly 45 percent of all prescriptions in the U.S.(But not in India) today are filled using generic drugs. This can save as much as 90 percent over the cost of brand-name medications.
Fact 1. A generic drug is made with the same active ingredients and is available in the same strength and dosage form as the equivalent brand-name product.Generic drugs produce the same effects in the body as the brand-name drugs, because both contain the identical active ingredients. The difference is in the name. The brand
name is the name under which the product is sold and is protected by a patent for up to 20 years. When the patent expires, other manufacturers can produce the generic equivalent of the brand and sell it under its generic name.
Fact 2. The manufacturing process of all drugs is strictly regulated by the Indian government and the same standards are met by all manufacturers. The FDA & CDSCO (Food and Drug Administration) inspects drug manufacturers and recalls any marketed products that do not meet production standards. The FDA can even stop the manufacture of products until the firm shows that it can make and test its drugs in a way that meets the high standards of the FDA. Each manufacturing plant is also inspected by the FDA and must be in compliance with the FDA standards known as Good
Manufacturing Practices.
Fact 3. A generic drug meets the same stringent performance and bioequivalence standards set by the U.S. federal government as the brand-name drug. Each generic drug is laboratory-tested to ensure that the same amount of drug will be absorbed into the bloodstream as with the brand-name drug. "Since 1984, no generic drug has been approved in the U.S. unless it has been shown to have the same rate and amount of active drug absorbed as the brand-name drug."
Fact 4. A generic drug is as safe and provides the same therapeutic effects as the
brand-name product for patients of all ages.As a group, generic drugs have no proven age-related side effects that are different from brand-name drugs. Generics have been shown to be as safe as brand-name drugs and work no differently in children or the elderly.
Fact 5. Many of the generic drugs approved by the Govt are manufactured by companies that also make brand-name drugs.Many more generic drugs will become available as brand-name drugs, such as Vasotec® and Prilosec®, lose patent protection.
Fact 6. Health care professionals strongly support the use of generic drugs. The American Medical Association, the largest organization of medical doctors, states
that generic drug products are acceptable for use by the American public. Most hospitals routinely use generic drugs for treatment of their patients.
Fact 7. There were 77 generic drugs on the list of the top-200 drugs sold in the
U.S. in the year 2000. In fact, the top drug sold as a new prescription in 2000 was the generic version of Vicodin®. Additionally, four of the top ten sellers by prescription volume in 2000 were generics.
Fact 8. The American public spent over $130 billion dollars on prescription drugs in 2000.With the price of generic drugs averaging 15 to 60 percent less than the cost of brandnamedrugs, the American public can save billions of dollars by using generic drugs.
Overall, this savings can help control the cost of health care in the India without reducing the quality offered to patients.
Fact 9. Generic drugs provide a valuable way for senior citizens to lower their
cost of prescription medications.Senior citizens represent 13 percent of the U.S. population, and they account for 25 to 33 percent of the prescription drugs used each year. Senior citizens use an average of 11 different prescriptions per year. Because many people over the age of 65 have fixed incomes, a considerable amount of savings can be gained through the use of generic drugs.
Fact 10. The decision to use generic medications is ultimately made through the cooperation of your physician, your pharmacist, and yourself.
Ask your physician or pharmacist if any of the prescription medications that you are
currently taking can be filled with a generic alternative. Once you begin using generic drugs whenever possible, you can start to reduce prescription drug costs while maintaining the same strength, dosage, and quality as the brand-name drug.
This flyer has been designed to provide you with important and accurate information
about generic drugs and their use. Please consider the option generics provide for those who want to receive high quality medications at considerably lower prices. Once you decide generics may be the right choice for you, please discuss with your physician or pharmacist the possibility of receiving equivalent generic medications for your prescriptions. Bear in mind that nearly 45 percent of all prescriptions in the U.S.(But not in India) today are filled using generic drugs. This can save as much as 90 percent over the cost of brand-name medications.
Fact 1. A generic drug is made with the same active ingredients and is available in the same strength and dosage form as the equivalent brand-name product.Generic drugs produce the same effects in the body as the brand-name drugs, because both contain the identical active ingredients. The difference is in the name. The brand
name is the name under which the product is sold and is protected by a patent for up to 20 years. When the patent expires, other manufacturers can produce the generic equivalent of the brand and sell it under its generic name.
Fact 2. The manufacturing process of all drugs is strictly regulated by the Indian government and the same standards are met by all manufacturers. The FDA & CDSCO (Food and Drug Administration) inspects drug manufacturers and recalls any marketed products that do not meet production standards. The FDA can even stop the manufacture of products until the firm shows that it can make and test its drugs in a way that meets the high standards of the FDA. Each manufacturing plant is also inspected by the FDA and must be in compliance with the FDA standards known as Good
Manufacturing Practices.
Fact 3. A generic drug meets the same stringent performance and bioequivalence standards set by the U.S. federal government as the brand-name drug. Each generic drug is laboratory-tested to ensure that the same amount of drug will be absorbed into the bloodstream as with the brand-name drug. "Since 1984, no generic drug has been approved in the U.S. unless it has been shown to have the same rate and amount of active drug absorbed as the brand-name drug."
Fact 4. A generic drug is as safe and provides the same therapeutic effects as the
brand-name product for patients of all ages.As a group, generic drugs have no proven age-related side effects that are different from brand-name drugs. Generics have been shown to be as safe as brand-name drugs and work no differently in children or the elderly.
Fact 5. Many of the generic drugs approved by the Govt are manufactured by companies that also make brand-name drugs.Many more generic drugs will become available as brand-name drugs, such as Vasotec® and Prilosec®, lose patent protection.
Fact 6. Health care professionals strongly support the use of generic drugs. The American Medical Association, the largest organization of medical doctors, states
that generic drug products are acceptable for use by the American public. Most hospitals routinely use generic drugs for treatment of their patients.
Fact 7. There were 77 generic drugs on the list of the top-200 drugs sold in the
U.S. in the year 2000. In fact, the top drug sold as a new prescription in 2000 was the generic version of Vicodin®. Additionally, four of the top ten sellers by prescription volume in 2000 were generics.
Fact 8. The American public spent over $130 billion dollars on prescription drugs in 2000.With the price of generic drugs averaging 15 to 60 percent less than the cost of brandnamedrugs, the American public can save billions of dollars by using generic drugs.
Overall, this savings can help control the cost of health care in the India without reducing the quality offered to patients.
Fact 9. Generic drugs provide a valuable way for senior citizens to lower their
cost of prescription medications.Senior citizens represent 13 percent of the U.S. population, and they account for 25 to 33 percent of the prescription drugs used each year. Senior citizens use an average of 11 different prescriptions per year. Because many people over the age of 65 have fixed incomes, a considerable amount of savings can be gained through the use of generic drugs.
Fact 10. The decision to use generic medications is ultimately made through the cooperation of your physician, your pharmacist, and yourself.
Ask your physician or pharmacist if any of the prescription medications that you are
currently taking can be filled with a generic alternative. Once you begin using generic drugs whenever possible, you can start to reduce prescription drug costs while maintaining the same strength, dosage, and quality as the brand-name drug.
Tuesday, August 23, 2011
Tuesday, August 2, 2011
Bridge Course Regulation -Bachelor of Pharmacy Practice (B.Pharm.Pr.)
Bachelor of Pharmacy Practice (Bridge course) Regulations 2010
(B.Pharm.Pr)
(Regulations framed under section 10 of the Pharmacy Act, 1948 (8 of 1948)
CHAPTER-I
Bachelor of Pharmacy Practice (B.Pharm.Pr.) shall consist of a degree certificate of having passed the course of study and examination as prescribed in these regulations, for the purpose of additional qualification to be entered in Register of Pharmacist under the Pharmacy Act, 1948.
Duration of the course. –
a) The duration of the course shall be of two academic years with each year spread over a period of not less than 180working days
Minimum qualification
i. A Pass in Diploma in Pharmacy Course from an institution approved by Pharmacy Council of
India approved under section 12 of the Pharmacy Act 1948.
ii. A registered Pharmacist under the Pharmacy Act.
iii. A Minimum of four years of pharmacy practice experience in a community or hospital
pharmacy –
a. A certificate from competent authority stating that the candidate is endorsed as Registered
Pharmacist in the Drug License of a Pharmacy as proof practice experience in case of
community pharmacist
b. A certificate from the Principal / medical Superintendent / competent person of the
Hospital/Health Unit stating that the candidate is working as a pharmacist will be accepted
as proof of practice experience in case of hospital pharmacist
iv. A no objection certificate from the employer in prescribed format (Annexure -A)
(B.Pharm.Pr)
(Regulations framed under section 10 of the Pharmacy Act, 1948 (8 of 1948)
CHAPTER-I
Bachelor of Pharmacy Practice (B.Pharm.Pr.) shall consist of a degree certificate of having passed the course of study and examination as prescribed in these regulations, for the purpose of additional qualification to be entered in Register of Pharmacist under the Pharmacy Act, 1948.
Duration of the course. –
a) The duration of the course shall be of two academic years with each year spread over a period of not less than 180working days
Minimum qualification
i. A Pass in Diploma in Pharmacy Course from an institution approved by Pharmacy Council of
India approved under section 12 of the Pharmacy Act 1948.
ii. A registered Pharmacist under the Pharmacy Act.
iii. A Minimum of four years of pharmacy practice experience in a community or hospital
pharmacy –
a. A certificate from competent authority stating that the candidate is endorsed as Registered
Pharmacist in the Drug License of a Pharmacy as proof practice experience in case of
community pharmacist
b. A certificate from the Principal / medical Superintendent / competent person of the
Hospital/Health Unit stating that the candidate is working as a pharmacist will be accepted
as proof of practice experience in case of hospital pharmacist
iv. A no objection certificate from the employer in prescribed format (Annexure -A)
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