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cGMP practices in herbal drug industry to build quality in pharma | 1792
Biochemistry & Pharmacology: Open Access

Biochemistry & Pharmacology: Open Access
Open Access

ISSN: 2167-0501

cGMP practices in herbal drug industry to build quality in pharmaceuticals


International Conference on Pharmacognosy, Phytochemistry & Natural Products

October 21-23, 2013 Radisson Blu Plaza Hotel, Hyderabad, India

Mahesh Burande

Accepted Abstracts: Biochem & Pharmacol

Abstract :

Good manufacturing practices in pharmaceutical industry are mandatory to build systems & improve quality in dosage forms. In herbal drug industry schedule, T emphasizes all these requirements and to build quality in herbal drugs modern methods such as vendor development, quality control, quality assurance, in process quality control, validation, calibration, standardization, and standard operating procedures should be implemented at every stage. This presentation describes the methodologies which are involved in building attitude to follow cGMP practices

Biography :

Mahesh Burande has 30 years of rich experience as a trainer and consultant to more than 100 pharmaceutical companies. His training programme inspires & ignites the minds of participant to build quality. His unique displays on cGMP, quality, productivity & positive attitude are appreciated by USFDA during various plant audits. IPER, where he is serving as Hon. Director has been awarded as most promising institute in the country in applied pharmacy education by Pharma Leaders award 2012.

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