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Prashant Deshpande, Head – Process Technology & Support, ACG World

Express Pharma

In this video: Prashant Deshpande, Head – Process Technology & Support, ACG World Topic: ACG Lab: Process Development and Optimisation made easy Key Takeaway: Process optimisation in pharma helps reduce manufacturing costs, increase efficiency, improve scalability, enable faster time to market, optimise resource allocation, boost product (..)

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13th HPAPI: Process Development for Highly Potent Drugs

pharmaphorum

Join the 13th HPAPI summit to learn about the latest advancements in process development for highly potent drugs. Explore topics like Annex 1, GMP guidelines, and drug development strategies.

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FDA’s Draft Guidance on the Q-Submission Program – A Step in the Wrong Direction

FDA Law Blog: Biosimilars

The guidance recommends that questions “that can be readily answered” based on the FDA reviewers “experience or knowledge” and that “do not require additional background information, an in-depth review, or other FDA staff involvement” can be done outside of the Q-Submission process.

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IDEA Series: Specialised Lectures in Emergency Medicine (SLEM) – A virtual conference to strengthen EM education in the developing world

ALiEM - Pharm Pearls

The Problem: Emergency Medicine (EM) in Pakistan has moved from developing to developed stage in the last decade [1]. It is an innovation that is based on a community of practice merged with the need-based assessment of a young EM residency program in a developing country. Originally developed by Marsh et al.,

Hospitals 161
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Prabhat Balyan, Manager-Business Development, Ami Polymer | Indore Pharma Summit 2023

Express Pharma

In this video: Prabhat Balyan, Manager-Business Development, Ami Polymer Topic: Polymeric solutions for pharma industry Key Takeaway: AMI Polymer, with its wide range of polymer solutions for different processes, can be a reliable partner for the pharma industry The post Prabhat Balyan, Manager-Business Development, Ami Polymer | Indore Pharma Summit (..)

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Krystal Biotech receives FDA approval for DEB topical gene therapy

Pharmaceutical Technology

Krystal Biotech has received approval from the US Food and Drug Administration for topical gene therapy VYJUVEK to treat dystrophic epidermolysis bullosa (DEB) in adults and in children aged six months and above. Topic sponsors are not involved in the creation of editorial content. It prevents epidermis adhesion to the dermis.

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UK medicines manufacturing to get innovation boost

European Pharmaceutical Review

Winners of a series of competitions centering on the aforementioned topics will obtain funding for UK medicines manufacturing. Theragenix aims to develop the world’s first dry powder gene therapy formulation for bone graft augmentation. The investment aims to improve vaccines and shorten the time it takes to produce medicines.