QP Module - Investigational Medicinal Products
- May 11, 2021 at 9:00 to May 12, 2021 at 17:00 UTC+01
- Location: Online
- Description:
All QPs need to understand the different Good Manufacturing Practice (GMP) requirements for commercial and Investigational Medicinal Products (IMPs), and the unique additional GMP requirements for IMPs. This two day interactive course examines the E - Created by: Christine Yarnall
- Tags: training, qp module, investigational medicinal products
All Events (110)
Further statistical tools for analytical scientists
- May 12, 2021 to May 13, 2021
- Location: Online interactive training
- Description:
Further statistical tools for analytical scientists
Modern analytical instruments are capable of producing a large amount of data. To interpret this data effectively requires the application of statistics. This course builds on the topics covered in
- Created by: Secretariat
- Tags: training, statistics, quality assurance
Good Distribution Practice
- May 17, 2021 all day
- Location: Online
- Description:
Updated and revised for 2020, this intensive course provides an extensive and detailed introduction to Good Distribution Practices in the Pharmaceutical industry. Covering best practices with practical examples and an overview of the regulatory fram - Created by: Christine Yarnall
- Tags: training, gdp regulations, quality management system
Responsible Person and GDP, Cogent Gold Standard Approved
- May 18, 2021 at 9:00 to May 20, 2021 at 17:00 UTC+01
- Location: Online
- Description:
RSSL has been providing Responsible Person training since 2012. Our latest Cogent Gold Standard Approved online and classroom courses incorporate the very latest regulatory aspects, best practice, customer and industry input.If your organisation alr
- Created by: Christine Yarnall
- Tags: training, responsible person training
New Medical Device Regulation (MDR) 2017/745
- May 24, 2021 all day
- Location: Reading UK
- Description:
Compliance with the forthcoming Medical Device Regulation (EU) 2017/745 (MDR) presents many new challenges to Medical Device manufacturers. Our in-depth MDR training is designed to help you and your team prepare for these challenges and transition sm
- Created by: Christine Yarnall
- Tags: training, medical device regulation, medical device
New Medical Device Regulation (MDR) 2017/745
- May 24, 2021 all day
- Location: Online
- Description:
Compliance with the forthcoming Medical Device Regulation (EU) 2017/745 (MDR) presents many new challenges to Medical Device manufacturers. Our in-depth MDR training is designed to help you and your team prepare for these challenges and transition sm
- Created by: Christine Yarnall
- Tags: training, medical device
QMS Lead Auditor for the Pharmaceutical Industry (IRCA Ref: PR330)
- May 24, 2021 at 9:00 to May 28, 2021 at 17:00 UTC+01
- Location: Online
- Description:
This 5 day fully residential course provides the most comprehensive certification for Lead Auditors in the Pharmaceutical industry. Fully accredited by IRCA and PQG, this is a highly customised Lead Auditor Training course that has been specifically
- Created by: Christine Yarnall
- Tags: training, qms lead auditor, gmp, pharma supplier standard
Active Pharmaceutical Ingredients Auditing
- Jun 8, 2021 all day
- Location: Online
- Description:
This course provides the knowledge and skills to enable effective auditing and reporting of audits on suppliers of active pharmaceutical ingredients (APIs). The course is focused on the requirements of ICH Q7 and EU GMP Part II and the expectations - Created by: Christine Yarnall
- Tags: training, auditing, good control laboratory practices
Good Distribution Practice, Online Bitesize courses
- Jun 11, 2021 from 9:00 to 10:30 UTC+01
- Location: Online
- Description:
These online bitesize courses will provide an extensive and detailed introduction to Good Distribution Practices in the Pharmaceutical industry, covering best practices with practical examples.
For those who are new to Good Distribution Practice for
- Created by: Christine Yarnall
- Tags: training, good distribution practices
Analytical Research Forum 2021 (ARF21)
- Jun 15, 2021 at 12:00 to Jun 16, 2021 at 17:00 UTC+01
- Location: VIRTUAL EVENT
- Description:
The Analytical Research Forum (ARF) provides the opportunity for early career researchers from analytical communities to present their work, alongside high profile analytical scientists. This flagship event of the Analytical Division will showcase cu
- Created by: Secretariat
- Tags: rsc, early career researcher, conference
SWIG: ACHIEVING NET ZERO – HOW DO WE USE MONITORING FOR ENERGY MANAGEMENT?
- Jun 16, 2021 from 13:00 to 16:00 UTC+01
- Location: Online interactive webinar
- Description:
Overview:
This webinar will cover the following themes:
· What are the key challenges to achieving Net-Zero by 2030 in the UK water sector ?
· Look at the key levers which will allow us to succeed.
· How can sensors optimise processes and systems to d - Created by: Secretariat
QP Webshow - Free Event
- Jun 17, 2021 all day
- Location: Online
- Description:
This is a packed day that explores everything involved in becoming a Qualified Person (QP). Attendees are encouraged to ask as many questions as they like to ensure that you leave with a clear understanding and can make an informed decision whether - Created by: Christine Yarnall
- Tags: training, qualified person, free event
Auditing to Pharmaceutical Standards
- Jun 21, 2021 all day
- Location: Online
- Description:
It is a regulatory requirement for organisations within the Pharmaceutical and Allied Industries to audit active pharmaceutical ingredient (API) manufacturers, suppliers of key excipients and packaging materials, and contracted-out laboratory service
- Created by: Christine Yarnall
- Tags: training, auditing to pharmaceutical standards, eu guide to gmp
Pharmaceutical Practical Auditing Skills
- Jun 23, 2021 from 9:00 to 17:00 UTC+01
- Location: Online
- Description:
This course provides an introduction to the requirements of internal auditing described in the international standard ISO 19011. Frequent opportunities to practice key steps are provided through role play in a no risk environment, with supportive fee
- Created by: Christine Yarnall
- Tags: auditing skills, gmp, training
QP Module - Pharmaceutical Quality Systems
- Jun 28, 2021 at 9:00 to Jun 30, 2021 at 17:00 UTC+01
- Location: Online
- Description:
The Qualified Person relies on the Pharmaceutical Quality System (PQS) to be able to fulfil their legal and operational responsibilities. This course provides a comprehensive overview of the requirements of the UK Study Guide. Scenarios and exercise - Created by: Christine Yarnall
- Tags: training, pharmaceutical quality systems, qp module, pqs
Biologically Derived Products - Testing and Manufacturing Challenges
- Jun 29, 2021 all day
- Location: Online
- Description:
The field of biologically derived medicines is expanding. With an increasing number of products being marketed, biological products bring unique challenges to the manufacturing process.
Biological products have unique challenges and constraints as co
- Created by: Christine Yarnall
- Tags: training, biologically derived products
QC Chemistry – Crash Course
- Jul 1, 2021 all day
- Location: Online
- Description:
A refresher course in Chemistry, applied to the QC Laboratory environment, for pharmaceutical professionals and trainee QPs who haven’t studied Chemistry beyond GCSE level. Designed as a preface to the QP Analysis and Testing Module.Chemistry is ess
- Created by: Christine Yarnall
- Tags: training, chemistry, trainee qps, qc chemistry
QC Chemistry - Crash Course
- Jul 1, 2021 all day
- Location: Online
- Description:
A refresher course in Chemistry, applied to the QC Laboratory environment, for pharmaceutical professionals and trainee QPs who haven’t studied Chemistry beyond GCSE level. Designed as a preface to the QP Analysis and Testing Module.
Chemistry is esse
- Created by: Christine Yarnall
- Tags: training, qc chemistry
Data Integrity and Electronic Records and Signatures
- Jul 6, 2021 all day
- Location: Online
- Description:
This course covers the key concepts of Record and Data Integrity and Electronic Records and Signatures, including the key regulatory requirements and expectations (including Annex 11 and Part 11, and related guidance), example citations, and pragmat
- Created by: Christine Yarnall
- Tags: training, data integrity, electronic records
Root Cause Analysis & CAPA
- Jul 7, 2021 from 9:00 to 17:00 UTC+01
- Location: Reading UK
- Description:
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 and made a regulatory requirement in Europe by Annex 20 of the Guide to GMP
- Created by: Christine Yarnall
- Tags: training, root cause analysis, capa