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 : In this Webinar, we will discuss: ▶ What is the principle of the ScanStation? ▶ Real-time counting: what are the advantages for my laboratory? ▶ How does the ScanStation integrate into my laboratory? ▶ Live Q&A more...

Summary : Jeremy Robertson, Global Solutions Manager - Microbial Identification Systems - bioMérieux explains how to achieve data integrity with automated ID systems. more...

Summary : This, first of its kind, fully interactive digital event features timely and topical presentations and panel discussions from 40+ global experts representing FDA, GSK, Kite Pharma, Novartis, Roche, and more. more...

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 : 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  virtual meeting hosted by Pharmig, as part of its bespoke series, for members and non-members, discusses continuous viable air sampling in response to changes in Annex 1 and cleanroom behaviours, qualification and support.  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 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 : Join this webinar to explore the new regulatory landscape for rFC and MAT as the assays gain global approval. rFC and MAT are no longer the "alternatives". 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 : Join PDA, USA for an in-depth exploration of the current state of development and regulatory thought for the advancement of advanced therapy medicinal products globally. 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 : Now delivered online 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 : The 3-hour virtual workshop/webinar is aimed at established and up-and-coming biofilm researchers and those with interest in the area of biofilms and their application in health and disease. more...

Summary : Representatives from industry, research organizations and regulatory authorities will 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 : This important annual event focuses on emerging issues related to the safety of building water systems.  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 : These 3 day workshops will focus on problems encountered in endotoxin testing, including resolving interference issues. 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 : Join Smi Group at their inaugural aseptic processing conference for an opportunity to explore aseptic facility design and operation to implement agile contamination control strategies. 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 : Are you looking for a rapid microbial detection method but aren’t sure where to start? Then join a Celsis^® Demo Day. more...

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

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 workshop will present practical approaches to rapid microbiology testing in the pharmaceutical industry. 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...

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