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CDMO Live 2025 to spotlight the future of pharmaceutical outsourcing in Europe

Express Pharma

Attendees will have access to exclusive networking opportunities, including the CDMO Live Boat Party, a city run in Rotterdam, a site tour of HALIXs biologics facility, and practical workshops addressing industry challenges. “Manufacturing strategy has become a board-level priority,” said Chris Kilbee, co-founder of CDMO Live.

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Pharmaceutical Continuous Manufacturing: Right for some products, but not all, and hurdles abound – workshop

Quality Matters

For certain drug substance and drug product manufacturing processes, PCM can bring opportunities to enhance flexibility and efficiency, lower production costs, cut environmental footprints, accelerate scale-up when needed, improve process control, and reduce potential quality issues, workshop participants reported.

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Understanding opportunities and challenges for SMEs after breather on Schedule M deadline

Express Pharma

In a notification issued earlier this month, The Union Health Ministry has granted a one-year extension to small and medium-sized pharmaceutical companies to upgrade their facilities as per the revised Schedule M of the Drugs and Cosmetic Act.

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5 Strategies to Strengthen Relationships with HCPs

Pharma Marketing Network

Developing strong and meaningful relationships with Healthcare Professionals (HCPs) is vital for healthcare organizations, pharmaceutical companies, and medical device manufacturers alike. Consider organizing workshops, webinars, or conferences to share valuable medical insights, research, and developments.

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Manufacturing pharmaceutical ingredients in Nigeria

Quality Matters

Pharmacopeia (USP), Bill & Melinda Gates Foundation, and Nigeria Sovereign Investment Authority to host a regional workshop on API manufacturing to help expand the sector. Other Nigerian-based pharmaceutical companies are also expanding production.

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Psychedelic medicines: are they gaining traction in Europe?

European Pharmaceutical Review

Legislative hurdles aside, in the same way as any other pharmaceutical companies, psychedelics companies will need to obtain regulatory approvals in the countries where they will carry out clinical trials or market products. 8 Where does Europe stand globally in psychedelic medicines development?

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Exclusive Pharma Microbiology interview with Maria Jose Lopez Barragan, formerly at FDA

pharmaphorum

FDA regulator and founder of Barragan BioConsulting, where she offers Regulatory and Compliance consulting services to pharmaceutical companies globally. Interested in joining the conference and workshop you can register your place for only US$499 (conference) and US$299 (workshop) www.microbiologyeastcoast.com/PR9.