LUPIN POSTS TWO FOLD INCREASE IN Q4 NET

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GMP Inspection Preparation Checklist: A Tool for Internal Auditing

This management report includes more than 650 items organized in three sections covering all aspects of quality manufacturing.

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Biological Risk Evaluation and Management for Medical Devices

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Events

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Jan 29

Developing Pharmaceutical Investigational Brochures & Annual Reports: Secrets to Practical Succes...

Jan 30

Regulating Software Used by Life Science Manufacturers: Is it a Medical Device or Not?

Feb 13

Building a World-Class Drug Supply Chain: Tips for Compliance and Digital Transformation

Feb 19

Medical Device Risk Management: Prepare for the Winds of Change

Mar 20

Medical Device Complaint Management: Escape the Labyrinth

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Conducting Advanced Root Cause Analysis and CAPA Investigations

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FDA Clears Sofregen’s Voice Augmenter

The device uses a proprietary single-use catheter delivery system.

Allergan, St. Regis Tribe Seek SCOTUS Review of Sovereign Immunity Case

The Patent Trial and Appeal Board ruled last year that Native American tribes cannot use sovereign immunity as a defense against inter partes reviews.