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Check out the latest CMIC White Papers! CMIC Group is contract research organization supporting companies in pharmaceutical developments.

[White Paper] How the fast-changing R&D pipeline is amplifying the importance of adaptable CROs

The story of CMIC’s rise from being a startup in [...]

By |2023-10-05T10:04:24-04:00June 10th, 2020|Comments Off on [White Paper] How the fast-changing R&D pipeline is amplifying the importance of adaptable CROs

[White Paper] Recommendations on the interpretation of the new European Medicines Agency Guideline on Bioanalytical Method Validation by Global CRO Council for Bioanalysis (GCC)

Senior representatives of GCC member companies have thoroughly evaluated and discussed the new European Medicines Agency (EMA; July 2011 [1]) Guideline on Bioanalytical Method Validation (BMV), during the 4th GCC (23 October 2011, Washington DC, USA) and 5th GCC (14 November 2011, Barcelona, Spain) Closed Forums. These North American and European events provided a unique opportunity for CRO leaders to openly share opinions and perspectives and to agree on unified bioanalytical recommendations specifically in relation with the new EMA guideline.

By |2023-10-01T01:56:12-04:00November 20th, 2019|Comments Off on [White Paper] Recommendations on the interpretation of the new European Medicines Agency Guideline on Bioanalytical Method Validation by Global CRO Council for Bioanalysis (GCC)

[White Paper] Recommendations on: internal standard criteria, stability, incurred sample reanalysis and recent 483s by the Global CRO Council for Bioanalysis

The 2nd Global CRO Council (GCC) for Bioanalysis Closed Forum was held on 15 April, 2011 in Montreal, Canada. In attendance were 45 senior-level representatives from 39 CROs on behalf of eight countries.

By |2023-10-05T09:51:34-04:00November 20th, 2019|Comments Off on [White Paper] Recommendations on: internal standard criteria, stability, incurred sample reanalysis and recent 483s by the Global CRO Council for Bioanalysis

[White Paper] Recommendations on Incurred Sample Stability (ISS) by the Global CRO Council (GCC)

The topic of Incurred Sample Stability (ISS) has generated considerable discussion within the bioanalytical community in recent years.  The subject was an integral part of the 7th Annual Workshop on Recent Issues of Bioanalysis (WRIB) held in Long Beach, California, USA, in April 2013, and at the Global CRO Council (GCC) meeting preceding it.  

By |2023-10-05T15:14:59-04:00November 20th, 2019|Comments Off on [White Paper] Recommendations on Incurred Sample Stability (ISS) by the Global CRO Council (GCC)

[White Paper] GCC Recommendations on Bioanalytical Method Stability Implications of Co-administered and Co-formulated Drugs

An Open Letter written by the GCC describing the GCC survey results on stability data from co-administered and co-formulated drugs was sent to multiple regulatory authorities on 14 December 2011. This letter and further discussions at different GCC meetings lead to subsequent recommendations on this topic of widespread interest within the bioanalytical community over the past two years.

By |2023-10-05T10:03:25-04:00November 20th, 2019|Comments Off on [White Paper] GCC Recommendations on Bioanalytical Method Stability Implications of Co-administered and Co-formulated Drugs

[White Paper/Infographic] The Changing Face of Global Clinical Trials: Asia-Pacific as an Ideal Destination for Specialty Biopharma

The contract research organization (CRO) market in the Asia-Pacific (APAC) region is the fastest- growing in the world, with revenue expected to increase at a 20% compound annual growth rate (CAGR) from 2016 to 2021 compared with the rest of the world’s 11.4% CAGR.

By |2023-10-31T12:11:15-04:00September 30th, 2019|Comments Off on [White Paper/Infographic] The Changing Face of Global Clinical Trials: Asia-Pacific as an Ideal Destination for Specialty Biopharma

[White Paper] How To Run Successful Clinical Trials In Japan

There is no longer any excuse not to include Japan as an integral part of any global clinical-development program for either pharmaceuticals or medical devices. With a more receptive climate for both starting and running trials, an improved infrastructure for clinical research, and significant advances in accelerating drug approvals, Japan is now firmly on the global development map.

By |2023-10-05T10:05:20-04:00September 25th, 2019|Comments Off on [White Paper] How To Run Successful Clinical Trials In Japan
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