Summary : Whether you need a foundation for cleanroom microbiology or are looking for a refresher, this on demand webinar will outline critical components and current best practices. more...

Summary : Performing an endotoxin test for product release may not be enough to ensure patient safety, the monocyte activation test performed with the PyroMAT™ System detects both endotoxin and non-endotoxin pyrogens. Watch our Webinar to learn more.
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Summary : Environmental monitoring of air, surfaces and personnel in aseptic areas can be complex, particularly in terms of culture media and regulatory requirements including GMP, ISO norms and pharmacopoeia. Join Merck's on-demand webinar to see how we can help guide you through.  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. more...

Summary : This two hour live webinar will explore and define the necessary elements in the development and implementation of a data integrity program and consider how to maintain quality systems with the aim of ensuring compliance. more...

Summary : The objective of this live, interactive training webinar is to explore the various issues surrounding the history of B. cepacia and its Complex and examine solutions to common microbiological problems. more...

Summary : Including a review of the new 2018 MHRA data integrity definitions & guidances and the FDA’s most recent draft guidance this live interactive webinar will examine the issues surrounding data integrity lapses. more...

Summary : This 90 minute webinar available live and on-demand will address the issue of CAPA effectiveness. more...

Summary : Join this live, interactive training webinar and learn how to develop a suitable cleaning and disinfection program to ensure the safety of both sterile and non sterile pharmaceutical products more...

Summary : Explore the management of OOS practices, how to minimize deviations, OOT, OOS and CAPA and how to tackle these situations should they occur. Also determine how FDA and ICH regulations and guidances may impact them. more...

Summary : This practical course covers basic issues in cleaning processes in pharmaceutical manufacturing, and the validation of those processes. more...

Summary : This 90 minute webinar, available live and on demand, will deal with best practice in aseptic technique and cleanroom behaviour more...

Summary : The objective of this live training webinar is to explore the more common microbiological aspects of data deviation investigations, and how FDA and ICH regulations and guidances impact them. more...

Summary : The objective of this live training webinar is to explore the more common microbiological aspects of data deviation investigations, and how FDA and ICH regulations and guidances impact them.  more...

Summary : This comprehensive live training webinar is designed to provide a comprehensive review of selected regulatory documents as they relate to sampling and sampling recovery, dirty hold time, clean hold time, microbiological issues and validation maintenance.  more...

Summary : This live training webinar will also examine a variety of the issues surrounding raw materials to include what materials should be tested and to what extent during Phase 1, 2 and 3.  more...

Summary : As the industry’s leading hands-on cleaning validation training, IVT’s Cleaning Validation conference goes beyond best practices and solution oriented approaches
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Summary : This training will be focused on the understanding of the classical methods described in the pharmacopeia and the currently available rapid microbiological method technologies, the regulatory requirements, the validation strategies and implementation plans. more...

Summary : The aim of this training course is to facilitate a deeper understanding and provide insights into the Aseptic Processing environment, and to go beyond what is commonly covered in books on that subject.  more...

Summary : The objective of this live and interactive training webinar is to explore the use of various modes of sterilization and learn how they may be used within your current manufacturing operation to provide both sterile components and final product. more...

Summary : The conference will address the key challenges in manufacturing and aseptic processing of Biological and Advanced Medicinal Therapeutic products (ATMPs) considering challenges in GMP compliance and application of Quality Risk management and new regulatory requirements  more...

Summary : This years microbiome therpeutics US will explore how to transform microbiome concepts into market ready therapeutics more...

Summary : This course will feature the development of suitable analytical methods and a systematic validation of analytical methods for cleaning residues.  more...

Summary : This training course about virus filtration will provide the attendees with a profound understanding about the current state of the art around this topic.  more...

Summary : After completion of this 3 day workshop you will be able to run microbiological test procedures in a compliant and at the same time efficient manner. more...

Summary : The Pharmaceutical Sterilisation course provides delegates with a comprehensive understanding of moist heat and dry heat sterilisation processes from theoretical foundation through to the practical aspects of validation and biological indicators. more...

Summary : Pharmig has developed this comprehensive learning opportunity to help explain the current state of rapid methods within the pharmaceutical and biopharmaceutical industries.  more...

Summary : Join the premier event for the Microbiome community within APAC to advance the next generation of safe, effective and commercially viable microbiome based-therapeutics and nutritional products of the future. more...

Summary : During this three day workshop you develop strategies for a sustainable approach to performing microbiological testing procedures in compliance with current regulations. more...

Summary : Data integrity is a rapidly evolving discipline and needs to be engrained into the quality management system and culture. This conference will be comprised of interactive case studies, presentations, and roundtable discussions and best practices. more...

Summary : Delivered via a mix of, presentations, interactive sessions and workshops this short course will look into cleanroom behavior for aseptic services
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Summary : This live training webinar will review the various USP microbial methods and their relationship to method suitability, their inherent method, limitations, sampling quantities and volumes to assure that the test is being applied as appropriate per USP and how to interpret the final result. more...

Summary : Pharmig has developed this comprehensive learning opportunity to help explain the current state of rapid methods within the pharmaceutical and biopharmaceutical industries. more...

Summary : The objective of this live, interactive training webinar is to explore the various issues surrounding the history of B. cepacia and its Complex and examine solutions to common microbiological problems. more...

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

Summary : The course is suitable for all personnel involved in the management and operation of cleanrooms including Production Managers and Supervisors, Quality Assurance, Microbiologists, Sterility Assurance Specialists and Sterility Assurance Engineers. more...

Summary : This excellent 3 day event focuses on how to address ongoing industry needs like process control, investigation strategies, and improving lab efficiency.  more...

Summary : Discover more about the latest scientific, technological and commercialisation trends and how they are driving forward skin microbiome research. Presentations address host-microbe interaction, skin disease, emerging technologies, interventional and cosmetic advances, and regulatory considerations. more...

Summary : This two day event will focus on future regulatory, commercial and legal challenges of biosimilars more...

Summary : The course provides an overview of the concept of qualification and validation as described in Annex 15 to Eudralex Volume 4. more...

Summary : Conference Series LLC Ltd invites all the participants from all over the world to attend 3rd International Conference on Microbes and Beneficial Microbes during September 27- 28, 2019 at Toronto, Canada. more...

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

Summary : This course is designed specifically as an introduction to the important topic of pharmaceutical microbiology, it will review the impact of microbiology on many aspects of pharmaceutical manufacture and control.  more...

Summary : This stimulating course systematically builds up the knowledge of delegates over three intensive days covering the regulations and guidelines associated with GMPs and the expectations of the MHRA and FDA. more...

Summary : Learn the basic principles, processes and systems related to aseptic processing. Attendees will have the opportunity to do hands-on activities such as gowning qualification, facility cleaning and disinfection, performing aseptic processes in ISO 5 conditions and performing visual inspection. more...

Summary : The inaugural cleanroom technology conference will explore hot topics within cleanroom design and engineering, best practices and regulation, environmental and contamination control, and pharmaceutical microbiology. more...

Summary : This two hour live webinar discusses various regulations and how they impact non-sterile manufacturing to include the setting of specification, development of the process, holding times, preservation issues, cleaning, sanitization and the requirements for the testing of recovered microorganisms.  more...

Summary : This course is designed to provide guidance on how data should be controlled and managed from initial generation and recording, through processing, use, retention, archiving and retrieval. more...

Summary : This practical course covers basic issues in cleaning processes in pharmaceutical manufacturing, and the validation of those processes. more...

Summary : This two-day course is set up as a highly interactive event with hands-on lab training sessions and workshop sessions on risk analysis and design of Environmental Monitoring. The lecture part will cover current regulations, methods and devices.  more...

Summary : This Honeyman Training is a must for anyone seriously involved in this aspect of Pharma Manufacturing.  Highlighting the essentials of designing, building, owning and operating pharmaceutical water systems. Design of water purification, storage and distribution system with illustrated examples.  more...

Summary : The objective of this live, interactive webinar is to explore and define the necessary elements in the development and implementation of a data integrity program, in a manufacturing/laboratory environment, and understand how to maintain quality systems. more...

Summary : This course provides an introduction to the requirements of systematic failure investigation (FI) and corrective and preventive action (CAPA) practices as described in ICH Q9. more...

Summary : IVT’s 25th Annual Validation Week promises an Inside Look at the Regulatory Landscape - CSV, Data Integrity, Data Privacy and More… more...

Summary : This live, interactive training webinar will assist those involved in the development of a process or the manufacturing of a product to explore water, as a raw material in a GMP environment, the requirements for potable water, purified water, water for injection and steam. more...

Summary : The objective of this live and interactive training webinar is to assist those involved in the development of a process or the manufacturing of a product to explore water, as a raw material in a GMP environment,  and to assure that they are meeting the current USP, EP, JP and FDA requirements. more...

Summary : Clinicians, Pharmacists and Microbiologists will benefit from this Seminar at Liofilchem.  MIC Test Strip (MTS) HEAR courses comprise an interactive two day session with lectures and laboratory work. more...

Summary : The 14th Annual PDA Global Conference on Pharmaceutical Microbiology continues the ongoing tradition of addressing the opportunities and challenges most relevant to the future of microbiology in today’s global market. more...

Summary : Now in it's eighth year the conference will explore recent advances in antibiotics. more...

Summary : This pharmaceutical validation course covers topics such as the development of regulatory expectations, effective cleaning procedures, process validation and control of these procedures.  more...

Summary : The 2019 PDA Rapid Microbiological Methods Workshop will provide attendees with an overview of the current landscape for rapid method validation strategies, implementation opportunities, and global regulatory approval processes. more...

Summary : The UK’s only trade exhibition dedicated to the laboratory industry Lab Innovations gathers laboratory manufacturers & suppliers of lab equipment and professionals all under one roof.  It's a great opportunity to meet decision makers and showcase your latest innovations.  more...

Summary : This unique event will bring together experts to advance scientific knowledge about microbiome in pregnancy and neonatal, interpret recent research and analyze real-world case-studies.  more...

Summary : This live interactive training webinar will help you to gain an enhanced understanding of the monitoring of bioburden, its inherent methods, and limitations to assure that the test is being applied as appropriate per United States Pharmacopeia and how to interpret the final result. more...

Summary : This satellite symposium will give you a scientifically sound introduction into the field of Rapid Mycoplasma testing with a specific focus on NAT and more specifically on qPCR methods.  more...

Summary : PharmaLab 2019 will cover various topics in 8 interesting conferences, a pre-conference workshop and lectures on analytics, bio analytics, microbiology and R&D. more...

Summary : With a diverse and interesting programme of presentations, debates and discussions and a Gala dinner this years Hot Topics in Pharmaceutical Microbiology, now in it's 27th year promises to be an event not to be missed. more...

Summary : With a theme of "challenges and strategies in sterile manufacturing" the Pharma Microbiology Congress promises an interesting and informative meeting. 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 : This ECA education course is designed to cover all important aspects of controlling microbiological contamination. It ranges from sources of contamination to validation of cleaning and disinfection processes and training of operators. more...

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

Summary : The manufacture of sterile products is subject to additional GMP controls and relies heavily on the competency and knowledge of everyone involved in the process. This course covers all key aspects of sterile product manufacture, for both aseptically prepared and terminally sterilised products. more...

Summary : The use of isolators ensures improved microbiological safety of sterile medicinal products, particularly in aseptic manufacture. This training course will help you in the qualification of these systems and the validation of the production processes. more...

Summary : This workshop is an opportunity to learn about the general principles of real-time PCR, including experiment setup and data analysis.  Delegates will benefit from practical experience and hands-on training with DNA-extraction and real-time PCR setup. 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. more...

Summary : The course addresses environmental monitoring for the manufacturing of both sterile and non-sterile products. more...