Summary : Our microbiology expert provides you with the latest updates on ISO 11133 standard and practical lab tips for your daily culture media handling, preparation, shelf-life, and performance testing.  more...

Summary : Join this webinar to see the automation solutions Neutec Group has to offer for your microbial testing laboratory. more...

Summary : Environmental Monitoring (EM) and cleanroom qualification are critical parts of the EU’s guidance on good manufacturing practices.  This on-demand webinar focuses on what's expected to change in the next revision of Annex 1. more...

Summary : Environmental Monitoring (EM) and cleanroom qualification are critical parts of the EU’s guidance on good manufacturing practices.  This on-demand webinar will consider more about the changes and requirements as well as where the principles of QRM must be applied.  more...

Summary : Environmental Monitoring (EM) and cleanroom qualification are critical parts of the EU’s guidance on good manufacturing practices.  This on-demand webinar is the first in a series focusing on EM and cleanroom qualifications, as well as quality control and bioburden testing. more...

Summary : This comprehensive live instructor-led training series of three webinar sessions is designed to provide a comprehensive review of selected regulatory documents as they relate to cleaning validation. more...

Summary : This free 60 minute Lonza webinar, also available on-demand, features bioprocess optimization through automated, aseptic sampling for bioreactors enabling control of product quality attributes and accelerated development times. more...

Summary : View this on-demand webinar to learn about environmental monitoring expectations, required microbiological testing measures, and finished sterile product testing for medical devices. more...

Summary : This 30 minute live webinar on 25th June will examine effective sample preparation for microbial analysis.  Also available on-demand. more...

Summary : This series of webinars, available on-demand, provides a comprehensive overview of the proposed changes to Annex 1, the EU's guidance on manufacturing sterile medicinal products. more...

Summary : The objective of this live training webinar is to obtain an enhanced understanding of USP <71> Sterility Tests, its inherent method, limitations, sampling quantities and volumes to assure comply with United States Pharmacopeia more...

Summary : Understand what the global expectations are for equipment qualification and validation and how to write and execute sound protocols for equipment qualification (IQ, OQ, PQ) and process validation. more...

Summary : This live interactive training webinar will address the key differences in implementing GMP requirements in a clinical, versus a commercial, manufacturing setting. more...

Summary : RSSL has been providing Responsible Person training since 2012. Our latest Cogent Gold Standard Approved online and classroom courses incorporate the very latest regulatory aspects, best practice, customer and industry input. more...

Summary : This live interactive webinar will discuss different phases of the drug development process and the role of the QC laboratory. more...

Summary : Pharmigs first European event has been re-scheduled to September 2020.   more...

Summary : For a comprehensive understanding of sterilisation processes, cGMP requirements and industry expectations for routine operation, monitoring and control, course provides practical examples of how techniques are applied to ensure reliability in full compliance with EU and US regulatory requirements. more...

Summary : This course will cover the main types and sources of micro-organisms and the issues associated with them in relation to both sterile and non-sterile pharmaceutical production. more...

Summary : Purified water is the #1 raw material in pharmaceutical manufacturing, used at almost every stage of the manufacturing process.  This industry-leading Honeyman Training course is a must for anyone involved in designing, building, owning and operating pharmaceutical water systems.  more...

Summary : With 220 exhibitors Forum LABO LYON will showcase laboratory innovations to over 3,000 researchers, engineers, buyers and expected decision-makers from the Rhône-Alpes / Auvergne, Switzerland, Italy and Belgium. more...

Summary : This course provides a detailed and structured introduction to cleaning validation along with up to the minute details of current best practice, cGMP expectations, industry trends and regulatory issues for both the EU and US markets.  more...

Summary : Now delivered online the 15^th Annual PDA Global Conference on Pharmaceutical Microbiology continues the ongoing tradition of addressing the most relevant opportunities and challenges to the future of microbiology in today’s global market.  more...

Summary : Join the Microbiome Movement and explore the global advances in translational microbiome research whilst meeting like-minded peers who are continuing to understand the causal and therapeutic potential of the 'second genome'. more...

Summary : This online workshop will present practical approaches to rapid microbiology testing in the pharmaceutical industry. more...

Summary : Delivered online for 2020, this years conference provides an opportunity for industry experts to discuss the latest advances and challenges in the area of Pharmaceutical Microbiology.  more...

Summary : Delegates will have an opportunity to gain and understanding of the challenges in GMP manufacture of biological products and the very different regulatory aspects. more...

Summary : This course is designed to give non-microbiologists a comprehensive introduction to microbiology so that they can engage in the required control measures, investigations and corrective actions. more...

Summary : The Pharma Microbiology Congress aims to create an annual meeting for microbiology/sterility assurance experts and pharma professionals to share last updates on regulatory trends, innovative technologies, and best practices for the manufacture and control of sterile API and medicinal products. more...

Summary : An overview of bio-pharmaceutical manufacturing, ideal for introducing bio-pharma processes as a start-up manufacturer and for established manufacturers expanding into biotechnology. Gene therapy, monoclonal antibodies, clinical trials, scale-up, cell culture processing, purification, separation. more...

Summary : This course has been completely revised and includes many new topics including the use of Disposable Technology, RABS and Isolator Technology, ETO, Gamma, E-beam, CAPA/OOS, Sterile Product Inspection Techniques and Risk Management Workshops. more...

Summary : The course will provide a basic understanding of the Risk Management of Contamination (RMC) system that can be utilised for the control of contamination during manufacturing operations in cleanrooms. more...

Summary : This three day GMP Workshop is designed for microbiologists, managers and supervisors of pharmaceutical microbiological laboratories.  Delegates will learn how to run microbiological test procedures in a compliant and time efficient manner. more...

Summary : This live training webinar will discuss laboratory deficiencies and how to minimize OOS and OOT investigations. more...

Summary : This important annual event focuses on emerging issues related to the safety of building water systems.  more...

Summary : The American society for microbiology are proud to invite you to attend ASM Microbe 2020.  Delegates can expect to hear the latest advances in microbiology, connect with peers on new collaborations, meet people with similar interests and gain exposure to new techniques. more...

Summary : The theme for this years's conference is novel approaches and best practices for tackling current pharmaceutical industry contamination control chalenges. more...

Summary : With a focus on facility design and operation to implement agile contamination control strategies join SMi Group at their inaugural aseptic processing conference. more...

Summary : SMi invites you to join them in addressing the challenges, for the next generation of cleanroom technology and engineering, by bridging the gap and sparking conversation. more...