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FOPE & PharmaState Academy host Session 12 of the PULSE series

Express Pharma

Jayakumar also spoke about the detailed procedures and SOPs needed for investigating market complaints and how these systems should be integrated into a companys overall quality management system. The panel also noted the importance of mock recalls to test readiness for real-life scenarios.

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Optimising project management in pharma: 8 steps toward efficiency

Express Pharma

As a Contract Development and Manufacturing Organisation (CDMO), companies such as Bachem play a crucial role in supplying Active Pharmaceutical Ingredients (APIs) to biotech and pharmaceutical companies, with responsibilities including raw materials management, process development and validation, production, purification, and delivery.

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AI in Medical Affairs: Revolutionizing Life Sciences with AI-Powered Tools

Viseven

Scientific communication : Drafting slide decks, scientific responses, medical information letters, and training content using generative models, ensuring scientific accuracy and compliance in messaging and content.

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Supporting the pharmaceutical industry – how a CDMO can help

European Pharmaceutical Review

It represents one of the highest-risk stages in sterile pharmaceutical manufacturing” The importance of fill and finish cannot be overstated. It represents one of the highest-risk stages in sterile pharmaceutical manufacturing, where even minute contamination can render entire batches unusable.

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From data to impact: How real-world evidence will transform healthcare

pharmaphorum

Skip to main content Monday 7 July 2025 BlueSky linkedin youtube rss User account menu Subscribe Channels Channels Digital Market Access Oncology Patients R&D Sales & Marketing Spotlight on Content type Content type Digital -News -Views & Analysis -Deep Dive -Webinars -Podcasts -Video -White Papers -Event Market Access -News -Views & (..)

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Top AI Tools for Pharma Marketers: Boosting Compliance, Content, and Customer Engagement

Pharma Marketing Network

In practical terms, this means fewer legal escalations, faster campaign launches, and improved documentation for FDA or EMA audits. Conclusion AI is transforming the way pharmaceutical companies communicate, educate, and engage. By proactively managing risk, AI frees up human reviewers to focus on nuancenot repetition.

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U.S. Pharmaceutical company improved quality of overall documentation saving time and filing delays

Syner-G

Challenge Syner-G was contracted by a US Pharmaceutical Company to help improve the quality of submission documentation generated during the manufacture of a Drug Substance intended for Phase II trials. Results Syner-G reviewed each documentation and provided suggestions/comments/guidance to the CDMO to bridge the gaps observed.