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Dr Mansukh Mandaviya inaugurates 27 greenfield bulk drug park projects and 13 medical devices plants under the PLI Scheme

Express Pharma

Dr Mansukh Mandaviya, Union Minister for Chemicals & Fertilizers and Health & Family Welfare virtually inaugurated 27 greenfield bulk drug park projects and 13 greenfield manufacturing plants for medical devices recently. The following are the details of bulk drug plants inaugurated : Sl. Dr. Arunish Chawla, Secretary; Dept.

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Ensuring Product Safety: U.S. FDA Guidance on Testing High-Risk Drug Components for Diethylene Glycol and Ethylene Glycol

Quality Matters

Excipients, or inactive ingredients, in a drug formulation are critical components, comprising up to 90% of a drug formulation by volume and serving important functions such as improving stability and increasing bioavailability for targeted drug delivery. The guidance document is available here: [link].)

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Reflecting on five years of quality control for nitrosamine impurities

European Pharmaceutical Review

This challenge is further compounded by increasingly complex drug formulations and global ingredient supply chains that stretch manufacturers’ capabilities in testing and control of impurities. 1 Nitrosamines are not new or unknown impurities. USP has also launched the Nitrosamines Exchange – a community hub and virtual platform.

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5 Qualities to Look for in Your Veterinary Pharmacy Partners

epicur

Traditional 503A compounding pharmacies and 503B outsourcing manufacturers both serve as important partners for veterinary practices, providing patient-specific prescriptions and manufacturing bulk drugs for in-practice use and dispensing when allowed by state regulations. Our blog gives you a comprehensive look at the two. Read the Blog 3.

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There has been a strong wave of M&A activity in Indian domestic formulations space

Express Pharma

Not surprisingly, a lot of activity has been in the pharma sector, across multiple sub segments including domestic formulations, API/CDMO and nutraceutical ingredients. Pharma B2B has witnessed consistent M&A activity, especially in the Active Pharmaceutical Ingredient (API) segment. By when will we see the results of such moves?

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Warehouse material handling for pharmaceutical industry

GMPSOP

When bulk raw materials arrive in bulk carriers (e.g., Some bulk carriers may also be used for the transportation of different bulk materials (i.e., cleaning certificate) before you should accept the bulk materials. tank trucks or railroad tank cars) you should check those are not pressurized.

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Six steps process to implement change control management

GMPSOP

– Estimation of resources required to bring about the change. Such as product name, batch number, expiry period, ingredients, composition, concentrations, dosage information, storage condition, age restriction, etc. . – The anticipated plan including a schedule for task completion and proposed date (s) of implementation.