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New PIC/S Guidance Documents published

Written by Wolter

Published: 27 June 2018

SERIALIZATION OBLIGATION

Written by Wolter de Vries

Published: 24 January 2018

EMA: How can a GMP non-compliance statement be lifted?

Written by Wolter de Vries

Published: 26 September 2017

ICH Q11 Q&A reaches Step 4

Written by Wolter de Vries

Published: 08 September 2017

Applications to host EMA Headquarters

Written by Wolter de Vries

Published: 22 August 2017

Counterfeit Harvoni® Entered German Supply Chain

Written by Wolter de Vries

Published: 20 June 2017

EMA: Concept Paper on the Revision of Note on Quality of Water for Pharmaceutical Use

Written by Wolter de Vries

Published: 21 March 2017

China Food and Drug Administration: What’s new?

Written by Wolter de Vries

Published: 28 February 2017

PIC/S GMP Guide revised

Written by Wolter

Published: 30 January 2017

EMA revises Guideline on Process Validation for Finished Products

Written by Wolter de Vries

Published: 19 December 2016

On-site GMP Training

On-site GMP Training

To catch-up your
audit schedule?

To catch-up your
audit schedule?

Quality should be built in,

not to be added.

Quality should be built in,

not be added.

Quality should be built in,

not be added.

Quality should be built in,

not to be added.

Great Mountains (of) Paper (GMP)

Great Mountains (of) Paper (GMP)

Any advice on your compliance status

Any advice on your compliance status

Hyperion Pharma Consultancy

Hyperion Pharma Consultancy executes quality related projects and identifies and solves GMP related issues for the life sciences and food industry. Customers include large companies and sme’s.

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The Founder

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Free Top 10 CaPa’s

Latest news

New PIC/S Guidance Documents published

SERIALIZATION OBLIGATION

EMA: How can a GMP non-compliance statement be lifted?

ICH Q11 Q&A reaches Step 4

Applications to host EMA Headquarters

Counterfeit Harvoni® Entered German Supply Chain

EMA: Concept Paper on the Revision of Note on Quality of Water for Pharmaceutical Use

China Food and Drug Administration: What’s new?

PIC/S GMP Guide revised

EMA revises Guideline on Process Validation for Finished Products

Menu

Languages

Services

Contact Details

On-site GMP Training

On-site GMP Training

To catch-up your audit schedule?

To catch-up your audit schedule?

Quality should be built in,not to be added.

Quality should be built in, not be added.

Quality should be built in, not be added.

Quality should be built in, not to be added.

Great Mountains (of) Paper (GMP)

Great Mountains (of) Paper (GMP)

Any advice on your compliance status

Any advice on your compliance status

Hyperion Pharma Consultancy

Hyperion Pharma Consultancy executes quality related projects and identifies and solves GMP related issues for the life sciences and food industry. Customers include large companies and sme’s.

Free Top 10 CaPa’s

Latest news

Menu

Languages

Services

Contact Details

To catch-up your
audit schedule?

To catch-up your
audit schedule?

Quality should be built in,

not to be added.

Quality should be built in,

not be added.

Quality should be built in,

not be added.

Quality should be built in,

not to be added.