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  - - Brazil’s resolution seeks to fast-track products approved by recognized health authorities
      
      Blog
      
      17th November 2022
      
      PDA Annex 1 Workshop: Six Key Takeaways from the Final Annex 1
      
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      14th November 2022
      
      PharmaLex strengthens foothold in regulatory services after merger with strategic consultancy BlueReg
      
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      13th November 2022
      
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Webinars related to Medtech

IVDR webinar

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Meeting your requirements for the IVDR Technical Files

10th November 2022

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The regulatory and business importance of medical device post-market surveillance

28th July 2022

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Software Medical Devices – Considerations for Regulatory Compliance Success

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Remediation and Preparations: a recap of current state and what is next for Medical Devices and In Vitro Diagnostics in Europe under MDR and IVDR

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Get Your Design in Control

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Medical Device Risk Management for Patient and Product Safety

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TGA (Australia) Approaches for Accelerated Medicine Approvals

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Medical Device Software: Current Developments in the Regulatory World

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Medical Device Clinical Evaluation Reports (CERs) -What you need to know

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Strategic and Scientific Consultancy
Integrated Product Development
Bringing Innovations to Market
Global Headquarter / End-to-end Outsourcing
Local Affiliate Services
Merger and Acquisition Support

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