ABOUT US

Inpharmatis is a full range of regulatory services and electronic solutions for the Life Science industry.

Our team of highly experienced experts is highly committed to supporting you during this difficult time as best as possible by continuing to provide full pharmaceutical product life-cycle management over the whole European & CIS market in comprehensive regulatory affairs services to Life Science Industry including Drug Development and Vigilance services to pharmaceutical, medical device, food supplement, cosmetic and biotech companies, as well as providing medical writing, market access services, User Testing of Patient Information Leaflet (PIL testing/Readability testing) and a range of specific software to the pharmaceutical industry.

A multi-disciplinary team of qualified regulatory affairs consultants is at your disposal for all aspects of your marketing authorization applications for active substances and human medicinal products. Inpharmatis shall provide full regulatory support over the whole life cycle of your product.

	International and dynamic full-cycle consulting group in Life Sciences​			15+ years of proven experience operating in the EU and CIS region.​			Professional and highly qualified team​
	Full range of RA, PV, Quality and E-Solutions services for Life Sciences​			Partnership with leaders in pharmaceutical and medical device industry​			Proven compliance with high-quality standards​

SERVICES

Regulatory Affairs	Pharmacovigilance	GMP/GDP Auditing
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eSolutions for Industry and Regulators	Training	PIL Readability User testing
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EXPERIENCE

Medicinal Products​, API​ Medical Devices​ Food Supplements​ Cosmetic products​

GEOGRAPHICAL COVERAGE

Inpharmatis is partnering with clients in more than 70 countries and is ready to expand its expertise in other regions. Feel free to contact us to know how we can support you at: info@inpharmatis.com.

OUR TEAM

Inpharmatis brings together professionals with vast experience and the highest qualifications.

Years	High qualifications	Doctors, Pharmacists,	We speak more
of experience and	and	Chemists,	than 20
unique competencies	certificates	PhD holders​	different languages

OUR STRATEGIC PARTNERS

We have partnerships with several long-term business partners, to achieve successful results for our clients.

EXTEDO – Germany Global pharmaceutical industry-leading partner for the electronization and registration dossiers management and pharmacovigilance (including at the state level).				AGATHA – Japan Workflow electronization and lifecycle management cloud-based solutions of strictly regulated documentation in the field of pharmacovigilance, R&D, clinical research, and regulatory. ​
DOT Compliance – Israel Business process electronization cloud solutions to accelerate medications time to market.​				EPISTA Life Science – Germany Software solutions that automate and accelerate the validation of computer systems in the pharmaceutical industry.​