Summary : Each of these Chapters has relevance to each other and provides a significant knowledge base of microbiological requirements. Several of these have also been harmonized and permit one to not only follow the USP, but simultaneously meet the requirements of both the European and Japanese Pharmacopeia. more...

Summary : This interactive training course will provide valuable and practical insights into the design, installation and operation of barrier technology, specifically isolators. Learn about isolator design, operational requirements, cleaning and decontamination methods, and validation of isolators. more...

Summary : Obtain an enhanced understanding of USP <71> Sterility Tests, its inherent method, limitations, sampling quantities and volumes to assure that the test is being applied as appropriate per United States Pharmacopeia and how to interpret the final result. more...

Summary : Join experts from the pharma industry, key opinion leaders, end-users and regulators as they gather to share updates on hot topics and to learn from the practical experience of others. more...

Summary : This 3 day training course will provide a new perspective on Aseptic Processing. Introduce new thinking to your site and team for process validation and risk assessment. more...

Summary : Join this conference to hear experts discuss Endotoxin and Pyrogen testing more...

Summary : SMi proudly presents the 3rd Annual Pharmaceutical Microbiology West Coast Conference, in San Diego, USA, on the 5th and 6th of June 2019. more...

Summary : Nicht nur sauber, sondern rein: Was kann im Reinraum verbessert werden? Die Veranstaltung ist deutschsprachig, zwei Vorträge werden englisch präsentiert/ this event is German-speaking, two lectures will be presented in English. more...

Summary : ICH Q7 was established by US / EU and Japan to harmonize inspections in their respective countries but what is the impact on cGMP inspections? 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 : This course includes a comprehensive overview of the fundamental concepts utilized in the preparation of parenteral products. Participants work in small groups to prepare a small volume parenteral (SVP) product and perform relevant quality control tests and environmental evaluations.   more...

Summary : Hands-on training for sterile and non-sterile manufacturing excellence more...

Summary : This pharmaceutical validation course covers topics such as the development of regulatory expectations, effective cleaning procedures and process validation along with cleaning strategy and policy and maintenance of validated cleaning regimes. more...

Summary : Learn more about the latest thinking and compliance requirements around data integrity in the Pharmaceutical Industry more...

Summary : This Webinar discusses how a well implemented Laboratory Information Management System can support many aspects of an ISO/IEC 17025:2017 based management system 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 : This course is also intended to give a practical training on the use of the most common sampling standards: ISO 2859-1:1999 and ANSI/ASQ Z1.4. more...

Summary : A dynamic 24 hour conference with ‘TED talk style’ 20 minute presentations and discussions during the day to enable you to understand how people are navigating sales and marketing challenges in the scientific markets. more...

Summary : Hear case studies on pathogen detection, point-of-care, biosurveillance, sample prep technologies, and bio recovery.  more...

Summary : SAMPS is an association uniquely designed for people in commercial roles in Life and Material Sciences and associated organisations. It was formed in 2018 as the European branch of SAMPS formerly ACP-LS which has enjoyed 6 successful years in the more...

Summary : This training course will provide a foundational understanding of sterilization science that will then be applied in the selection of a cycle design approach, sterilization process development, process performance qualification and ongoing process control.  more...

Summary : How does the new standard impact upon laboratories that are already accredited? and how can you ensure staff adherence and ongoing compliance to minimize corrective actions arising from accreditation audits? more...

Summary : Now in it's fourth year this year's summit has a theme of "Pursuing disease causation to foster the creation of targetted microbiome-based therapeutics, biomarkers and diagnostics." more...

Summary : This course provides a comprehensive overview of the current regulatory requirements for the development, manufacture and approval of Advanced Therapy Medicinal Products (ATMP).  more...

Summary : Three types of record can be found in analytical laboratories working to GMP: paper, hybrid computerized system and electronic workflows with electronic signatures. Delegates will be taken through the process from analysis to generation of results to understand data integrity issues. more...

Summary : This two hour live training webinar will provide the learner with an enhanced understanding as well as a “refresher” of what requirements exist for the microbiologist throughout the production environment from in-coming through final release. more...

Summary : This auditing course will develop the understanding of what is required for a data integrity audit of a laboratory computerized system and then develop the principles, based mainly on workshops and discussions, of how to audit hybrid and electronic laboratory systems. more...

Summary : This one day course addresses environmental monitoring for the manufacturing of both sterile and non-sterile products. 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 objective of this two hour live training webinar is to obtain an enhanced understanding as well as a “refresher” of what requirements exist for the microbiologist from the end of production through final release for both non-sterile and aseptic produced products. 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 : This practical course covers basic issues in cleaning processes in pharmaceutical manufacturing, and the validation of those processes. 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 years microbiome therpeutics US will explore how to transform microbiome concepts into market ready therapeutics 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 : Pharmig has developed this comprehensive learning opportunity to help explain the current state of rapid methods within the pharmaceutical and biopharmaceutical industries.  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 : 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 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 : 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 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 : 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 : 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 : 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 : 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 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 : 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...