Summary : This intensive instructor-led annual GMP training series will consist of 6 live training sessions of 2 hours followed by 30 minutes of live Q&A each. It will include over 15 hours of live presentation and Q&A delivered periodically over the course of 3 months. more...

Summary : Now in it's 22^nd year this year's Superbugs and Superdrugs will focus on non-traditional approaches in the fight against antimicrobial resistance. more...

Summary : This one day fast track intensive workshop will cover contamination issues from facility design to product release and how to develop a contamination control strategy. This will address, ATMP Guidance, EU Annex 1, EU Annex 2, FDA’s Aseptic Guidance and more.  more...

Summary : This one day fast track intensive workshop will cover contamination issues from facility design to product release and how to develop a contamination control strategy. This will address, ATMP Guidance, EU Annex 1, EU Annex 2, FDA’s Aseptic Guidance and more. more...

Summary : Pharmig will hold their first virtual conference on the topic of Pharmaceutical Water Systems.   Agenda includes: Trouble shooting water systems - What auditors look for, How to react to OOS results, What is the data more...

Summary : This course outlines the principles of planning, qualification and operation of cleanrooms & barrier systems and their associated HVAC systems in the GMP environment. more...

Summary : The objective of this intensive training course is to enable participants to understand critical issues during the design, qualification and routine operation of pharmaceutical water systems. more...

Summary : This webinar is part of a complimeny series provided by RSSL and hosted by Dr Tim Sandle. These webinars are designed to guide you through the complexities around sterile products manufacturing, control, testing and release. more...

Summary : Are you looking for a rapid microbial detection method but aren’t sure where to start? Then join a Celsis^® Demo Day. more...

Summary : The content of the webinar will focus on the practical and how to best thoroughly accomplish an effective CAPA system.  This webinar also highlights the various regulations governing CAPAs and how CAPAs are successfully initiated and managed. more...

Summary : This intensive annual live training program on the topic of USP Microbiological General and Information Chapters will consist of 7 live training sessions of 2-hour presentation time followed by 30 minutes of live Q&A each. more...

Summary : This webinar will help you understand the critical ingredients for conducting an effective root cause analysis. You will learn about FDA expectations, tools and techniques, and tips for conducting and documenting root cause analysis. 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 : Honeyman Training courses highlight the key and essential points of designing, building, owning and operating pharmaceutical water systems. Basic design of water purification, storage and distribution system elements will be outlined, with illustrated examples. more...

Summary : The A2LA Tech Forum has grown to become one of the largest, multidiscipline events in the accreditation industry, attracting attendees from over 12 different industries, including automotive, environmental, pharmaceutical, calibration, and more. more...

Summary : Updated for 2020, this 3 day course systematically builds up the knowledge of delegates over three intensive days. It covers the regulations and guidelines associated with GMPs and the expectations of the MHRA and FDA. 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 : Delivered by Veronika Wills, Manager, Technical Services, Associates of Cape Cod, this workshop will provide an in-depth overview of the use of synthetic (non-animal based) reagents for bacterial endotoxin testing. more...

Summary : This event offers you a unique possibility to understand, ongoing regulatory requirements and the development of microbiological methods for quality and process control as well as learning from recent experiences in microbial contamination control. more...

Summary : This webinar is part of a complimeny series provided by RSSL and hosted by Dr Tim Sandle. These webinars are designed to guide you through the complexities around sterile products manufacturing, control, testing and release. more...

Summary : Brought to you by Microrite, this two day course will inform delegates how to conduct robust investigations into microbial and particulate contamination.  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 : Managing sterilisation processes is critical to the manufacture of terminally sterilised and aseptically prepared products. Special requirements minimise the risks of contamination, with much depending on the skill, training and attitudes of the personnel involved. more...

Summary : This course provides an extensive introduction to the regulatory requirements governing pharmaceutical clean room operation, and details the aseptic filling and terminal sterilisation methods for producing sterile products. more...

Summary : This conference provides a unique opportunity to learn about the new regulatory requirements of the revised second Draft of Annex 1, the impact on aseptic manufacturing and the challenges relating to quality aspects. more...

Summary : Delegates will learn about the development and validation of suitable analytical methods for cleaning residues. more...

Summary : This webinar is part of a complimeny series provided by RSSL and hosted by Dr Tim Sandle. These webinars are designed to guide you through the complexities around sterile products manufacturing, control, testing and release. 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 : Brought to you by Microrite, this two day course will inform delegates how to conduct robust investigations into microbial and particulate contamination. more...

Summary : These 3 day workshops will focus on problems encountered in endotoxin testing, including resolving interference issues. more...

Summary : These 3 day workshops will focus on problems encountered in endotoxin testing, including resolving interference issues. more...

Summary : This interactive course examines why we have Good Manufacturing Practice (GMP), its legal status and the key GMP issues surrounding pharmaceutical manufacture such as documentation, training and facilities. more...

Summary : This meeting will concern itself with advanced technologies and methods for global health and biodefense. 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 : Become an Aseptic Processing Subject Matter Expert with Honeyman's latest Specialist Pharmaceuticals Training Course more...

Summary : This two day course, delivered by the UK Anaerobe Reference Unit, Public Health Wales, provides a refresher in culturing, isolating and identifying clinically important anaerobes and takes a look at the latest technologies and techniques. 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 : LABWorld China will focus on R&D, inspection and analysis in the pharmaceutical, chemical and biotechnology areas, laboratory development and the implementation of Chinese Pharmacopoeia 2020.  more...

Summary : This meeting will provide an overview and updates on regulatory expectations and scientific investigations related to virus and TSE safety of biotechnology, plasma-derived, and cell-derived medicinal products.  more...

Summary : Delegates will learn how to avoid laboratory data integrity deficiencies and the protocols, methodology, and actions necessary to avoid regulatory action. more...

Summary : This event not only takes a deep dive into how companies comply with regulations, but also showcases how leading companies develop methods, validate procedures and generate data and information that lead to critical business decisions.  more...

Summary : Delegates will learn how to build and manage a stability program from the ground up. more...

Summary : Delegates attending A3P Microbiology will have an opportunity to inform themselves about rapid methods, online controls, microbiological gene therapy and current regulations.  more...

Summary : Representatives from industry, research organizations and regulatory authorities meet to discuss the many challenges in the manufacture of ATMP's, such as quality of raw materials, tech transfer, testing, registration and more. more...

Summary : After an introduction to the overall objectives, the course then covers process design, pitfalls and associated validation issues including sampling and testing. more...

Summary : Delegates joining this two day workshop will have an opportunity to learn how to implement a bioburden control strategy. more...

Summary : The course is focused on company responsibilities within a quality risk management system, and several investigational tools are explored to help build up knowledge of techniques that might be used by a company to provide a structure for systematic investigation of failure. more...

Summary : FEMS are delighted to invite delegates to attend this the 1st FEMS Conference on Microbiology structured to deliver the benefits of an international microbiology conference with the accessibility of a small to middle-scaled, affordable, regional conference. more...

Summary : Updated for 2020, this 3 day course systematically builds up the knowledge of delegates over three intensive days. It covers the regulations and guidelines associated with GMPs and the expectations of the MHRA and FDA. more...

Summary : Join delegates from the life science and cannabis industries at this informative congress.  Learn about regulatory compliance and best practices in the  formulation and evaluation of cannabis drug delivery. more...

Summary : Charles River QC micro summit is the premier three day thought leadership event for pharmaceutical and biotech industry professionals. 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 : Are you looking for a rapid microbial detection method but aren’t sure where to start? Then join a Celsis^® Demo Day. 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 : 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 : 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 : 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...