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Comparison of Indian medical device rules 2017 and EU medical device regulations 2017/745 and recommendations to industry.

By:

AGRAHARI, Nitika

Material type: Text

Text

TextDescription: ix,121ISBN:

NA

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Holdings
Item type	Current library	Home library	Collection	Call number	Status	Date due	Barcode
ACP-CDs	Acharya & BM Reddy College of Pharmacy	Acharya & BM Reddy College of Pharmacy	ACP-Drug Regulatory Affairs	615.19 AGR (Browse shelf(Opens below))	Not for loan		ACP-CD915

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Previous	615.190 0685 AJA Qualification of stability chamber	615.190 0685 OMA Prospective process validation for the manufacture of ketoprofen fast dissolving tablets	615.19 AGA An approach on current regulatory considerations of adverse event reporting & pharmacovigilance for biologics in India and US	615.19 AGR Comparison of Indian medical device rules 2017 and EU medical device regulations 2017/745 and recommendations to industry.	615.19 ALI Challenges in developing clinical trails for medical devices in US, EU and Indian market.	615.19 ANU The regulatory process for the import and export of pharmaceutical products in India.	615.19 CHA Text book of pharmaceutical regulatory science	Next

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