Utilizing our USP/ICH compliant, state-of-the-art laboratory, Nitto Avecia Pharma Services is capable of detection, profiling and control support of all three classes of residual solvents in drug substances, excipients, and drug products. Rapid analysis, identification, and quantification of impurities is completed in strict compliance of ICH guidelines.
Nitto Avecia Pharma Services is a premier contract development and manufacturing organization offering a comprehensive range of cGMP services including formulation development, parenteral manufacturing, and a complete package of CMC analytical services for small to large molecules and nearly all dosage forms
Current demand for sterile injectable drug product manufacturing is fed by multiple dynamics, and when the decision has been made to outsource there is a spectrum of options: niche CMOs with a sterile-injectable focus, large CMOs with end-to-end services for a variety of dosage forms, and one-stop-shops where both API and drug product manufacturing from development through commercialization can be supported.
Piramal Pharma Solutions is the contract development and manufacturing (CDMO) arm of Piramal Enterprises Ltd with a vast network of development and manufacturing facilities located in North America, Europe and Asia.
Nitto Avecia Pharma Services has in-depth experience with a wide range of drug delivery device technologies to offer your programs comprehensive technical support.
Do you need a contract development and manufacturing organization (CDMO) that will fill the gaps in the drug development process and focus on getting patients the treatments they need faster? Read how the team of experts at Singota is here to collaborate with you, customizing our services to meet your needs and hit your milestones.
Piramal Pharma Solutions (PPS) is pleased to welcome Ash Stevens LLC as a part of the Piramal Group. Leveraging five decades of Ash Stevens’s operational experience and technical expertise, Piramal’s service offering now includes High Potency API (HPAPI) development and manufacturing capabilities. Located in Riverview, USA, our state-of the-art FDA licensed cGMP facility offers a full range of scale and containment options for high potency API manufacturing.
Piramal Pharma Solutions is the contract development and manufacturing (CDMO) arm of Piramal Enterprises Ltd. with a vast network of development and manufacturing facilities in North America,Europe and Asia. We offer a vast array of services, which include Drug Discovery & Development, Clinical Supply of API & Dosage Forms, Commercial Manufacturing & Supply of API, KSMs, RSMs, Intermediates and Finished Dosage Forms. At Piramal, we are committed to fulfil our clients’ API development & manufacturing requirements, across all phases of the drug life cycle.
With nearly 30 years’ experience in supporting all compendial microbiological testing, Nitto Avecia Pharma Services has the in-depth experience, established quality systems, and expertise to best support your product life cycle at any stage.
With thousands of methods developed, validated, and/or transferred in support of IND/ANDA/NDA/BLA applications, Nitto Avecia Pharma Services’ scientific team has a proven track record with nearly all drug forms, substances, and products.
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