Contract R&D

Actylis offers GMP, biopharma and non-GMP specialty chemical custom ingredient research and development services by generating robust, practical and cost-effective processes for the preparation of specialty chemicals, excipients, and pharmaceutical ingredients. With decades of experience in problem-solving, our wide-ranging, global R&D team is highly skilled at timely development of scalable processes that focus on simplicity, robustness, and suitability for purpose. Throughout the years, we have provided GMP, biopharma and non-GMP specialty chemical custom ingredient solutions to a vast array of industries around the world. Capabilities: - GMP excipients and pharmaceutical intermediates- Non-GMP specialty chemicals with extensive experience in many different types of chemistry including chlorination, alkylation, Grignard chemistry, organo-metallic chemistry, hydro fluorination, halogen exchange, polymerization, etc.- Biopharma substances and intermediates for antiviral, cancerostatic and cardiovascular drug substances and for their key intermediates in the areas of Nucleotides, Nucleosides and their analogues. Actylis boasts comprehensive analytical capabilities including but not limited to purity testing, structural conformation, impurity identification and quantification, physical properties, stabilities, performance-based testing, comparative studies of products and raw materials. These analytical capabilities support our R&D teams as well as providing services to many well-known external partners. Check out our analytical service offerings here. Our Approach: Actylis' GMP, biopharma and non-GMP specialty chemical custom ingredient research and development services are composed of 5 main phases: 1. Initiation phase During this phase all your specific needs for the customized excipients, chemicals or raw materials are described and verified with our capabilities. This will already involve extensive communication betwee...