Enabling you to identify and mitigate the intrinsic risk in your operations, supply chains and business processes.
Evaluating how your products and services meet and exceed quality, safety, sustainability and performance standards.
Validating the specifications, value and safety of your raw materials, products and assets.
Highlighting outsourcing strategies supporting development of small molecule and biologics including GMP and CMC laboratory services at Biotech Outsourcing Strategies cmc 2017
During the Biotech Outsourcing Strategies (BOS) cmc conference and partnering event, Basel, 27th and 28th June 2017, meet with our team to learn how our innovative approaches and breadth of expertise can help you to overcome development challenges through outsourcing your GMP and CMC laboratory services needs.
We provide regulatory-driven, phase-appropriate, GMP and CMC laboratory services supporting API and Drug Product Outsourcing Strategies for NCE's and NBE's. Our GMP and cmc laboratory services support development programs for both small molecule and biologics and include method development and validation, pharmaceutical analysis, stability, formulation development, extractables and leachables studies, clinical trial material manufacturing, GMP QC testing, GMP batch release testing, impurity identification with risk assessment.
Our experts in inhaled product development, including all types of dry powder formulations and devices, nebulized solutions / suspensions and metered dose inhalation (pMDI) products and other novel respiratory delivery systems, will be at the event to discuss formulation strategies and OINDP testing requirements.
Our team will also be able to update you on support for manufacturing including particle investigation, material technologies, occupational hygiene, medical device testing, polymer/additive expertise and counterfeit medicines investigations.
Contact us if you are attending, and would like to meet during the 1 to 1 partnering meetings which provide a great opportunity to initiate contact or touch base on existing projects.
Biologics cmc Support Services
We offer world-class scientific support to clients focused on the development of biological medicines including biosimilars, proteins, monoclonal antibodies and antibody drug conjugates. Our programs include protein structural analysis, physico-chemical properties and potency testing for use in product characterization packages, comparability, stability or batch release.
John Todd, Business Development Manager – Biopharmaceutical Services, will present during the Biologics Track - Drug Substance Outsourcing on Tuesday, 27th June in the afternoon session from 3.00-3.15 pm
Presentation: "Successful Outsourcing: A CRO Perspective".
Contact us to request a copy of the presentation.
Learn more about us:
With a focus on providing expert regulatory-driven, formulation, analytical and bioanalytical services to support both small molecule and biologic medicines, our collaborative buyer/supplier partnerships are dedicated to helping clients overcome the challenges of drug development and manufacturing. Over the last 20 years, the Intertek network of Good Laboratory Practice (GLP) and Good Manufacturing Practice (cGMP) laboratories has provided high-quality technical services for some of the world’s largest and most innovative pharmaceutical companies.
About Biotech Outsourcing Strategies cmc 2017:
Established in 2008, BOS cmc is a leading partnering event for the CMC outsourcing community. Attendees include CMC outsourcing professionals from SME biotech, medium and large sized pharma, CMO/CDMOs and CROs offering analytical/testing capabilities.
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