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JoBurmester.com

We are here to help you maintain ethical and regulatory standards in compliance with ICH E6(R3), ICH E8, EMA, FDA and MHRA when conducting Clinical Trials with Investigational Medicinal Products (CTIMPs). We can also cover the specific requirements for Advanced Therapy Investigational Medicinal Products (ATMPs/ATIMPs), for example Gene Therapy.

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  • ICH GCP & Regulatory Update: Essential Insights for Clinical Trial Professionals

    Webinar

    Discover the latest regulatory changes in clinical trials. A critical live webinar for clinical research professionals to stay compliant and informed about new ICH GCP requirements.

    £180

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