Lipid excipients and delivery systems for pharmaceutical development: A regulatory perspective☆
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Markets for Pharmaceutical Products
Pharma Live, , Regulatory Affairs, 0
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Leveraging Third-Party Audits in Pharma/Biotech Industries – Courtesy (Pharmaceutical Manufacturing)
Pharma Live, , Regulatory Affairs, 0
Those of us in the competitive and highly regulated pharmaceutical, biotechnology and medical device industries understand the need to...
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A REVIEW ON GOOD MANUFACTURING PRACTICE (GMP) FOR MEDICINAL PRODUCTS
Pharma Live, , Regulatory Affairs, 0
ABOUT AUTHORS:Vikash Kumar Chaudhari1*, Vijay Yadav2, Praveen Kumar Verma1, Amit Kumar Singh21Department of Pharmaceutical Chemistry,2Department of Pharmacognosy,Kunwar Haribansh Singh...
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Drug Firms Warned Over Non-Registration With Online Database in India! – Courtesy (NDTV)
Pharma Live, , Regulatory Affairs, 0
With only 41 out of top 100 pharmaceutical firms responding to its direction to register for online database, the...
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A REVIEW ON STABILITY GUIDELINES BY ICH AND USFDA GUIDELINES FOR NEW FORMULATION AND DOSAGE FORM
Pharma Live, , Regulatory Affairs, 0
ABSTRACTStability guidelines for new drug substance and new pharmaceutical formulations as per ICH and USP for the evaluation and...
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Pharmaceutical industry regulation undermines NICE drugs appraisal work – Courtesy (Pharmanews.eu)
Pharma Live, , Regulatory Affairs, 0
Government policies that support UK pharmaceutical science and enhance export income are costing the NHS millions and undermine the...
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Medical Writing Services in Asia: Recent Developments and Trends – Courtesy (PAREXEL)
Pharma Live, , Regulatory Affairs, 0
Authored by: Dr Julia Cooper, Vice President, Head of Global Medical Writing Services, PAREXEL In an increasingly complex and...
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Roche moves closer to US filing for alectinib – Courtesy(PMLiVe)
Pharma Live, , Regulatory Affairs, 0
Positive data from two trials of Roche’s ALK inhibitor alectinib in lung cancer will be used to support a...
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