We will be continuing to attend relevant events for the remainder of 2019 as they are always a great opportunity to meet with customers and stay informed of key trends and regulatory changes within the pharmaceutical and healthcare industries. We appreciate the chance to offer advice or guidance on the solutions we can provide customers with for their specific environmental monitoring or process validation requirements.
We are scheduled to attend the following events for the remainder of 2019:
13th & 14th November 2019 – Nottingham Belfry Hotel
Pharmig’s annual conference provides the latest update and hot topics in pharmaceutical microbiology. The agenda includes: Recent findings and expectations from the MHRA; Contamination control strategy; Microbiological considerations for ATMPs; Challenges in viable colony counting by visual inspection of growth media as part of environmental monitoring programs; Round up of new standards and regulations during the past year; The new Annex 1 and its impact on environmental monitoring activities and more.
PDA Ireland Chapter: Visual Inspection Event and AGM
22nd November 2019 – Carton House, Co. Kildare, Ireland
The PDA Ireland Chapter discuss the latest developments in relation to visual inspection, including requirements, practical implementation and future technologies. Industry experts will share their perspectives and best practices including use of latest technology. Regulatory experts will discuss the latest pharmacopoeial requirements and regulatory expectations.
Panel discussions, case studies and networking opportunities will allow for full exploration of the topic.
NHS Pharmaceutical Quality Assurance and Technical Services Symposium
27th & 28th November 2019 – Bristol Marriott Hotel City Centre
The 2019 QATS Symposium is aimed at pharmacists and technicians working in pharmaceutical production, aseptic production, quality assurance and quality control environments within both the NHS and commercial sectors. This event offers a variety of presentations and workshops to educate and update delegates on current issues.
Topics covered will include: National aseptics review – phase 2 update; human microbiome; automated support in Aseptic preparation – options, issues and validation; MHRA update on deficiencies found in special units and Q&A session.
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The environmental monitoring processes and validation guide
Understand the key changes and challenges of the EU GMP Annex 1 draft revision.
What will it mean for your environmental monitoring processes?