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2018 dates

Details of our 2018 pharmaceutical training courses with scheduled dates

Inspired Pharma 2018 course dates

Details and links to our pharmaceutical training courses dates – all courses held in Reading, UK unless stated otherwise – updated 1st April 2018.

Pharma GMP Auditor/ Lead Auditor

14th – 18th May 2018

25th -29th June 2018, Dublin

10th – 14th September 2018

5th – 9th November 2018, Manchester

3rd – 7th December 2018

Data Integrity: threats and issues

22nd May 2018

9th October 2018

 

 

 

Documentation and Records in GMP

19th September 2018

 

 

 

 

Good Manufacturing Practice

12th June 2018

17th October 2018

Pharma Internal Auditor

12th June 2018

17th October 2018

Pharma Problem Solving

27 – 28th November 2018

Sterile Products

19th – 20th June 2018

20th – 21st November 2018

About our courses …

Our range of highly praised and respected Pharmaceutical training courses feature:

  • A fresh approach to training
  • Using tutors who are excellent trainers
  • Without excessive use of PowerPoint slides
  • Using exercises and workshops to put the learning into practice
  • Giving you the facts that you need and how to apply them

We have a very wide range of existing pharmaceutical customers, small and large, and benefit from a great deal of repeat business from existing clients. We also focus on who the audience is – offering different styles of delivery and content depending on who we are training. This has resulted in superb levels of feedback from all organisational levels.

Our pharmaceutical training courses receive incredible feedback –  a small selection is shown below:

“The way the tutors took us through the course was fantastic. They picked us up and the enthusiasm and passion made me a big fan of this course”.

QA Auditor, GLAXOSMITHKLINE

“Thank you for the week. I thoroughly enjoyed the course and came away with a lot of information. I will be highly recommending Inspired Pharma.”

QA Specialist, AZUR PHARMA

“I was worried that the course would be very monotonous and boring, and would involve hours of reading. I am glad to say that the course was anything but that! There are many tutors that could do with a lesson in teaching from you guys. I really do admire the way you make the course interesting and involve the delegates in active learning.”

QA Officer, PHARMASERV

“A tremendous learning experience”

Director, Pharmaceutical Consulting Group

See our Testimonials page for more feedback on our pharmaceutical training courses. To keep in touch or to access our taster courses for GMP, GDP and QP training please complete the panel below.

Find out about our course ranges

GMP Training

QMS Training

GDP/RP Training

GMP Compliance

QP Training

GDP Compliance

About Inspired Pharma

We help people in pharma organisations to continually improve their regulatory systems to gain competitive advantage and ensure compliance.

We offer a wide range of highly praised and respected classroom and online training courses and also provide our global pharma clients with consultancy support. Our classroom courses are available on a public schedule and also can be customised for inhouse delivery at a client site.

Quick Links

Find your way quickly to any  part of our website by selecting any of the links in this section

Online courses available anytime anywhere

Data Integrity

Good Distribution Practice (GDP)

Good Manufacturing Practice (GMP)

Pharma Quality Management Systems module

QP Medicinal Chemistry & Therapeutics module

QP Quality Management Systems module

Each course typically consists of 10-20 minute chapters of content followed by a quiz based assessment. The QP courses feature tutor assessment too. The learning is accessed over the internet using desktop computers, laptops, tablets and even smartphones.

Why not subcsribe to our mailing list to try a free Taster  of these courses to see if they are of interest?

Visit our Independent Reviews.io website

Ensure your team understand the importance of Data Integrity

Now Available - online Data Integrity training for your team Our 20-minute online Data Integrity training course will ensure your entire team understand the importance of Data Integrity and their...

New EU GMP Directive published

The European Union has published its new Directive for pharmaceutical manufacturing sites that is to replace the existing Directive (Directive 2003/94/EC) for human medicines. From having an initial look at the new Directive, here are a few comments.

What Pharma Companies Need to Know about Measuring Instrument Calibration

According to pharmaceutical cGMP (current Good Manufacturing Practice) guidelines, pharma companies need to conduct regular instrument calibration as part of their validation and qualification activities. This article gives an overview of what is involved.

Must, Shall and Should – the use of these words in GMP

What is the difference in meaning between these words in the context of GMP?, In this post I explain, using EU GMP as my point of reference, although as you will find out, there are occasions within EU GMP where the incorrect terms have been used.

Management Review – who, what, where and when?

The idea of Management Review meetings has only been a formal GMP requirement for the past 5 years or so. In the many visits that I do to pharmaceutical manufacturing sites I see these done – but rarely done well, which is a real shame. So what are these GMP Management Review meetings, why do we have them, what should be discussed, who should attend and how often should we have them?

2018 course dates

Details of our scheduled public course dates for 2018

Standards to use when auditing suppliers

If you are working to Good Manufacturing Practice (GMP) then you will need to audit many of your suppliers. GMP does not really tell you what pharmaceutical supplier standards you should or could use when auditing your suppliers this post lists of all the key standards to use when auditing suppliers including links to all of the key documents and authorities.

EU GMP Chapter 9: Self-Inspection – time for an update?

In the past few years eight of the nine chapters of EU GMP have been updated. However, Chapter 9 has not been updated at all. This is strange as GMP’s stance on Quality Management System thinking has evolved a lot of the past few years, so surely the requirements for the number one mechanism that you have to evaluate this system should be updated too? Here are my thoughts

News and Articles

Read our articles on  pharmaceutical regulatory developments as well as news about our pharmaceutical training courses.