𝗕𝗲𝘀𝘁 𝗣𝗿𝗮𝗰𝘁𝗶𝗰𝗲𝘀 & 𝗥𝗲𝗴𝘂𝗹𝗮𝘁𝗼𝗿𝘆 𝗦𝘁𝗿𝗮𝘁𝗲𝗴𝗶𝗲𝘀 – 𝗧𝗵𝘂𝗿𝘀𝗱𝗮𝘆 𝟱𝘁𝗵 𝗠𝗮𝗿𝗰𝗵 EPiC is pleased to highlight an upcoming webinar hosted by the Research Quality Association (RQA), designed for professionals involved in clinical trial operations, IMP oversight, and regulatory compliance. This comprehensive session…
The European Forum for Good Clinical Practice (EFGCP) are hosting a half day seminar this autumn on regulatory and ethical hot topics including practical considerations for ICH GCP E6(R3) Renovation, Investigational Medicinal Product (IMP) Regulations (EU and UK IMP considerations…
The Autumn Compliance Seminar had been given ‘In Principle’ CPD Certification EPiC Auditors have received notification from the CPD Certification Service that the further learning value and structure of our Autumn Compliance Seminar on 10th November 2022 conforms to CPD…
“you say tomato, I say tomahto” ???? Regardless of what we are calling our Autumn Compliance Seminar/ Symposium! This online conference will be a full day event delivered remotely, packed with a programme of informative sessions and presentations brought to…
EPiC Auditors Autumn Compliance Seminar: Thursday 10th November 2022 Here’s what our speakers have to say about the pharma compliance event; “How to achieve Regulatory compliance for small, new and innovative companies can seem an impossible task. How to maintain pharma…
With just over 3 weeks to go until the EPiC Autumn Pharma Compliance Seminar on Thursday 10th November 2022 we have released a copy of the whole day’s agenda. Here’s a summary of what is covered: Download the Agenda here:…
Registrations are now open for EPiC’s Autumn Compliance Seminar: Thursday 10th November 2022 Shaping a Pharma Compliant Future After the success of our GMP Symposium in February, EPiC Auditors are pleased to announce that we will be delivering a virtual compliance seminar…
We are very pleased to announce that Michelle Yeomans, GMDP Inspectorate Unit Manager at the MHRA will be delivering a Regulatory Update at the forthcoming GMP symposium. Michelle will be covering the Clinical Trials Regulation and what it means to…