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November 07, 2023

Newsletter Sponsor

GMP Carbon-14 Labeled API Manufacturing

Moravek is recognized internationally as a leading provider of GMP carbon-14 labeled APIs for use in early-phase clinical trials. Over 100 GMP APIs have been produced in compliance with FDA guidance, and all have successfully met client, CRO, and regulatory requirements.

Moravek offers outstanding CDMO capabilities and has substantial experience seamlessly coordinating concurrent progress of both CDMO and CRO activities.

	Industry News

TC BioPharm Selects CRO for Clinical Trials
TC BioPharm, a clinical-stage biotechnology company focused on developing allogeneic gamma-delta T ... read more »

Sygnature Discovery Invests $4.5M in Compound Management Storage System
Sygnature Discovery has incorporated an Azenta compound management storage system into its ... read more »

Noramco Acquires Cambrex Drug Product Business Unit
Noramco, a prominent worldwide producer of active pharmaceutical ingredients (APIs), renowned for ... read more »

Rentschler Biopharma Appoints Head of Quality Control for Laupheim Site
Rentschler Biopharma SE, a contract development and manufacturing organization (CDMO) specializing ... read more »

	Featured Articles

		Transitioning to Precision Medicine While pharma has produced some incredible blockbusters, it has largely remained unremarkable at the ... read more »

		Most Significant Risk Factors for Emerging and Mid-Market Biopharma Companies - Costly Clinical Trial Delays In 1820, a group of physicians, driven by concerns regarding the quality and reliability of ... read more »

	Featured Video

Documentary: Cell & Gene Therapy: Advancing the Next Generation of Pharmaceuticals
In this documentary, American Pharmaceutical Review and Pharmaceutical Outsourcing magazine spoke with industry experts to learn how cell and gene therapies are changing the healthcare landscape and ... read more »

On-Demand Webinar: The Pitfalls and Strategies for Pediatric Formulation Development
In this webinar you’ll learn common issues and strategies for pediatric formulations development as well as some of the various resources and regulatory bodies; Impact of age group, daily dose, and ... read more »

	Featured White Papers

		Whitepaper: Addressing Challenges with Clinical In-Use Testing of Biotherapeutics Lonza Drug Product expert Léa Sorret PhD explores Clinical In-Use Testing of Biotherapeutics in this white paper. Lea shares her expertise and ... read more »

		Whitepaper: The Viscosity Reduction Platform: Viscosity-Reducing Excipients for Protein Formulation Protein viscosity is one of the major obstacles in preparing highly concentrated protein formulations suitable for subcutaneous (subQ) injection. ... read more »

	More Services

Contract Manufacturing Learn More
Sterile Syringe Filling Services Learn More
Custom Synthesis Learn More

	Service Directory

Active Pharmaceutical Ingredient (API) Development Services Search More

Liquid Dosage Drug Formulation Development Services Search More

Pharmaceutical Microbiology Testing Services / Microbial Testing Services Search More

	Events

Bio-IT World Conference & Expo Europe
London, England – 11/29/2023
Bio-IT World Conference & Expo Europe unites a community of leading life sciences, pharmaceutical, clinical, healthcare, informatics, and technology ... event details »

PepTalk: The Protein Science Week
San Diego, CA – 01/16/2024
PepTalk 2024 will offer a comprehensive program presenting the latest research and development in the field of protein science and production. ... event details »

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