FROM CONCEPT TO MARKET

The aim of the Altiora Consulting is to be at hand to all the stakeholders involved in drug development and marketing, as well as post-marketing activities, capitalizing our long-lasting experience.   

Regulatory

Our experience ranges from clinical trial and marketing authorizations, price and reimbursement, medical technology, and regulatory strategy services to fixed drug combinations.

Quality Management

Through years of quality assurance activities and quality management system development and implementation we gained thorough insight of GCP, GLP and ISO standards. Our experience ranges from independent reviews and audits to GCP, GLP and ISO standards implementation.

Pharmacovigilance

Being aware of raising concerns and corresponding regulatory changes, it was decided to integrate Clinical Research & Post-approval Safety, as well as Medical Devices Safety into Altiora Consulting.

Legal

Supporting patent protection and intellectual property rights, merges and acquisitions, contracting and solicitation.

Trainings

Being focused on its human capital Altiora has developed it's training program.  Altiora Consulting is dedicated to share the knowledge by working on innovative methods trying to utilise modern technologies and combine them with traditional learning tools.

Science

Helping in concept and product development, study design, protocol and investigators brochure writing, scientific advice.

OUR SERVICES

PRECLINICAL

CLINICAL

POST-APPROVAL

We'd love to hear from you

CAREERS

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