AllExperts > Pharmaceuticals 
Search      
Pharmaceuticals
Volunteer
Answers to thousands of questions
 Home · More Pharmaceuticals Questions · Answer Library  · Encyclopedia ·
More Pharmaceuticals Answers
Question Library

Ask a question about Pharmaceuticals
Volunteer
Experts of the Month
Expert Login

Awards

About Us
Tell friends
Link to Us
Disclaimer

 
 
 
 
About Michael Anisfeld
Expertise
Disclaimer: SORRY BUT I DO NOT ANSWER QUESTIONS RELATED TO: DRUG ACTIONS/INTERACTIONS, INTERNET DRUG PURCHASES, RESULTS OF DRUG TESTS, IDENTIFYING DRUGS (FOR WHICH YOUR LOCAL PHARMACIST IS THE BEST PERSON TO CONSULT). My expertise is answering questions relating to pharmaceutical manufacturing and quality technologies, drug regulations and specifically GMP requirements

Experience

Past/Present Clients
UN agencies (UNFPA, UNICEF, UNIDO)
Governments (Australia, Canada, India, United Kingdon, United States
Companies - over 200 companies in 37 countries

 
   

You are here:  Experts > Health/Fitness > Pharmacology > Pharmaceuticals > Stability study samples

Pharmaceuticals - Stability study samples


Expert: Michael Anisfeld - 5/22/2007

Question
QUESTION: Dear Dr. Anisfeld
Regarding the withdrawn stability study samples at study points, what is the allowable period and at what condition samples should be stored before starting analysis?


ANSWER: 1, 2, and 3 months samples should be withdrawn and tested with 3 days of the target date;

6, 9, and 12 month samples should be withdrawn and tested within 7 days of the target date;

18, 24, 36 month samples should be withdrawn and tested with 14 days of the target date.

after withdrawal keep samples in refrigerator until tested,


---------- FOLLOW-UP ----------

QUESTION: Dear Dr. Anisfeld
Sorry for inconvenience, but I tried to search for this kind of information in the ICH guidelines but I found nothing, is this scenario a company trend or there is an official reference?

Also I have a question regarding the GMP rules, during the packaging process of the pharmaceutical cream, is it accepted from the GMP point of view to unpack the defected (rejected) tubes and refill the contents? If its accepted, does it considered reprocess action?

Thanks and best regards


Answer
The timings I provided came from an old FDA guideline from FDA's Office of General Drugs. Regretfully this is no longer on the FDA website, and I no longer have the original.

Yes, you can open the tubes and repackage them if you can figure out a way to do this without in any way contaminating the recycled cream - an almost impossible job.

Additionally due to the economics, this almost never done.

Add to this Answer   Ask a Question


 
User Agreement | Privacy Policy | Kids' Privacy Policy | Help
Copyright  © 2008 About, Inc. AllExperts, AllExperts.com, and About.com are registered trademarks of About, Inc. All rights reserved.