Medicines, Medical Devices, Cosmetics, Food Supplements

Your one-stop-shop solution in pharma & healthcare

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Everything in One Place

Your Personalized  Pharmacy

What are you looking for?

Are you into…

Outsourcing ?

You can entrust all QA, RA, PV and Medical related responsibilities for your Pharma & Healthcare business in Benelux to IN2Pharma. We act as RP or QP to the authorities as required and ensure compliance in the respective area of expertise.

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Seeking advice ?

If you need specific advice on a topic in one of our domains, you can benefit from our
expertise and experience on an ad hoc basis.

Getting the project done ?

Workload too high?  Absent colleagues? Need for a back-up?  Our dynamic and well-trained consultants get the work done for you!  Whether it is short or long term, at your site or from our offices in Kampenhout.

WHAT ARE OUR areas of expertise?

We are into …

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Regulatory Affairs

We can support you in obtaining and maintaining Marketing Authorizations for medicinal products, medical devices, cosmetics and food supplements.

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Publicity & Compliance

We support you in ensuring compliance of the promotional materials for your medicinal and healthcare products and of the promotional activities you sponsor or organize. 

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Vigilance

At IN2Pharma, we offer a wide range of vigilance services. We can help your company to comply with the legal obligations for pharmacovigilance, materiovigilance, cosmetovigilance and a food safety plan for food (supplements).
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Medical writing & training

IN2Pharma can provide you with a full range of medical support. We write or review scientific and medical reports, we create and present medical training courses.

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Quality Assurance

We are specialized in the good distribution practices (GDP), Good Manufacturing Practices (GMP) (importation and batch release) and have an extensive knowledge of the applicable local legislation.

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Our DNA

We are NOT just another consultant

Who We Are

We are … in2pharma !

Discover Our IN2Pharma DNA
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Regulatory Intelligence

and … we are into sharing !

Updates to the Dutch Medicines Act

Updates to the Dutch Medicines Act

The Netherlands Recent updates to the Dutch Medicines Act (Geneesmiddelenwet) of 8 February 2007 have been published. This Act defines the composition and responsibilities of the Medicines Evaluation Board (MEB) and regulates the licensing of manufacturers,...

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Update LCPV notification form

Update LCPV notification form

Luxembourg As part of the pharmacovigilance system, the marketing authorization holder has at its disposal, on a permanent and continuous basis, an appropriately qualified person responsible for pharmacovigilance. The person responsible for pharmacovigilance resides...

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Phone

+32 16 891 600

Location

Hof Ter Loonst
Terloonststraat 22
1910 Kampenhout
Belgium

Email

info@in2pharma.com

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