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The course was well organized and the staff was extremely reliable and competent. I’m totally satisfied with the course and I’m looking forward for next one! I strongly recommend it to anyone who wants to have a deeper understanding of the subject.
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...the information in a way that provides participants with a good overview of the quality and regulatory issues surrounding the development and production... Learn about: Quality Systems, Regulatory Compliance, Qualified Person (QP)...
...the information in a way that provides participants with a good overview of the quality and regulatory issues surrounding the development and production... Learn about: Quality Systems, Regulatory Compliance, Qualified Person (QP)...
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The course was well organized and the staff was extremely reliable and competent. I’m totally satisfied with the course and I’m looking forward for next one! I strongly recommend it to anyone who wants to have a deeper understanding of the subject.
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I was looking for a course to keep me updated and after attending the course, I can say that it was totally worth it! The course is well organized and easy to follow. I recommend it to anyone who wants to know all the latest changes in the field.
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...is designed to ensure a common framework for all ISO management systems. The changes in the new ISO 9001:2015 go further than structure, however... Learn about: Key changes, Industry insight, Pharmaceutical manufacturing...
...is designed to ensure a common framework for all ISO management systems. The changes in the new ISO 9001:2015 go further than structure, however... Learn about: Key changes, Industry insight, Pharmaceutical manufacturing...
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I was looking for a course to keep me updated and after attending the course, I can say that it was totally worth it! The course is well organized and easy to follow. I recommend it to anyone who wants to know all the latest changes in the field.
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...pharmaceutical ingredients (APIs). The course is focused on the requirements of ICH Q7 and EU GMP Part II and the expectations of regulatory bodies both in the USA and Europe... Learn about: Regulatory Compliance, Communication Skills, Decision Making...
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- Intermediate
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...All address details can be found on our website and in your Planning Your Visit pack received once you have booked a place. Please note all prices quoted... Learn about: Quality management, Quality Training, IT Auditing...
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- Intermediate
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...through processing, use, retention, archiving and retrieval. Data Integrity is assuming greater importance in cGMP, with both the FDA and European Regulatory... Learn about: Identify the data lifecycle elements, Java Programming, Design and qualification...
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- Intermediate
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...produce a better report and to make far better use of the time available. The emphasis is on planning, reader analysis, structuring the message and writing clearly... Learn about: Report editing, Report writing for Management, Report Writing...
Reviews on Reading scientific Services Limited (2)
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Recommended
CPD Day ISO 9001:2015 vs 2008 – What has changed?
Former Student
QP Module: Biotechnology Issues
Former Student
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Advantages of studying here
Once registered for a training course with us, you will have the support of a dedicated Client Relationship Manager and the most relevant subject matter experts who will be able to
answer your questions and challenge your thinking, during and after the course.
Areas of specialisation
- Qualified Person (QP)
- Good Manufacturing Practice (GMP)
- Responsible Person (RP)
- Auditing
- Stability
And more ............
Description
Our outstanding reputation as one of the most trusted pharmaceutical training providers, gives you the confidence that we are training your biggest asset to the highest standards. Investment in training not only gives your staff the key knowledge and skills they need but also ensures that they feel valued contributors to your organisational goals.
Our tutors are all industry specialists, bringing current and future thinking to the knowledge content, whilst the emphasis on problem based learning methods will guarantee that attendees leave with a pragmatic understanding of the subject, and the confidence to put it into practice in the workplace.