Engineering and Manufacturing training Reading

...in question Know how to obtain auditee cooperation and acceptance of findings... Learn about: Reporting on audits of suppliers, Enable effective auditing, Basic manufacturing techniques...

...The changes in the new ISO 9001:2015 go further than structure, however, providing a significant focus on risk based thinking, the role of leadership... Learn about: Industry insight, Risk Management, ISO 9001...

...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... Learn about: Pharmaceutical manufacturing, Pharmaceutical Research, European Politics...

...role people play in packing operations. It identifies major areas of risk and discusses how these can be removed or managed. Suitability This popular course... Learn about: Packaging technologists, Manufacturing Process, Packaging Operations...

...Suitability GMP for medical devices is the perfect course for people who are new to the medical device industry, the diagnostics sector or those working... Learn about: Quality Training, Pharmaceutical manufacturing, Manufacturing Process...

...Understand the testing techniques regularly used in pharmaceutical production operations Know what factors to consider when developing an environmental... Learn about: Good Manufacturing Practice (GMP), Environmental Monitoring, Manufacturing Process...

...and more extensive appreciation of pharmaceutical good manufacturing practices. Learning Outcome By the end of the course you will: Be able to find... Learn about: Goods exportation, Quality Training, Quality Systems...

...in today’s regulatory environment. Learning Outcomes At the end of the course you will: Understand the regulatory expectations Know how to evaluate validation... Learn about: Equipment qualification, Pharmaceutical manufacturing, Cleaning validation...

...lie within their own organisation and the potential reputation and cost consequences of non-compliance. Starting with a brief consideration of the... Learn about: Auditing documentation, Good Manufacturing Practice (GMP), Management Operations...

...execution, or validation of cleaning processes which may include operations managers and personnel, validation specialists, Quality Assurance and Quality Control managers... Learn about: Sampling and testing techniques, Analytical method validation, Pharmaceutical Plant Cleaning...

...this is the ideal opportunity for you to learn more about what is involved and decide on your next steps. Our QP Roadshow events are suitable for anyone... Learn about: Training Programme, Pharmaceutical manufacturing, Becoming a Qualified Person...

...Documentation is the cornerstone of any company’s quality management system and is an essential GMP requirement. It is critical that anyone dealing with... Learn about: Archiving and retrieval, GMP Documentation, Best Practice for Documentation...

...it will also be of direct relevance and benefit to packaging supervisors/managers, quality personnel working in packing departments, packaging technologists... Learn about: Printed Packaging Components, Packaging materials, Regulatory Compliance...

...Learning Outcomes At the end of the course you will: Understand the risks associated with sterile products Appreciate the requirements for contamination... Learn about: Aseptic filling and terminal sterilisation methods, Good Manufacturing Practice (GMP), Quality Training...

...experience or for those with experience but who wish to be updated with the latest application, particularly regarding science and risk based principles... Learn about: Good Manufacturing Practice (GMP), Risk analysis techniques, Quality Systems...

...to the ISO 9001 standard and the PQG’s Application Standards for suppliers to the pharmaceutical industry. Successful completion of this course provides... Learn about: Quality Training, ISO 9001, Pharmaceutical manufacturing...

...for external inspections by customers and regulators, manage an external inspection and respond to inspection observations including addressing any deficiencies raised... Learn about: Pharmaceutical manufacturing, Inspection Process, Quality Process...

...16 FAQ EMA guideline on quality of water for pharmaceutical use Mutual Recognition Agreement with America In addition there are a number of topics in the pipeline... Learn about: Data Integrity, Legislation and guidelines update, Quality Management Systems...

...It is also suitable for those who wish to refresh their skills. Learning Outcomes By the end of the course you will be able to: Understand the benefits... Learn about: External auditing, Internal Auditing, ISO 19011...

...for a supplier audit • Have the ability to create a structured approach in preparation for an API audit • Be able to conduct an API audit • Know how to... Learn about: Decision Making, Auditing documentation, Report Writing...