UMUT GUMUSBAS
© 2016 ANKOFIS. ALL RIGHTS RESERVED. Web Design by nihatozen
Intellectual Property Bsc
BD&Licensing BA
Regulatory Bsc
TR EN
Most companies, whether they are major multinational pharmaceutical corporations or small, innovative biotechnology companies, have specialist departments of Regulatory Affairs professionals – and those who don’t, rely on the expert advice of independent regulatory consultants to meet their obligations. AnkOfis keeps track of ever-changing legislation in Turkey. We also advise on the legal and scientific restraints and requirements, and collect, collate and evaluate the scientific data, the research and development companies are generating. We are responsible for the preparation and presentation of registration documents to regulatory agencies, and carry out all the subsequent negotiations necessary to obtain and maintain marketing authorisation for the products concerned. We give strategic and technical advice at the highest level to our clients on RA, BD and IP, right from the beginning of the development of a product, making an important contribution both commercially and scientifically to the success of a development programme and the client company as a whole.
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EUROPEAN COMPANY Company requested establishment of its TR subsidiary as well as regulatory submissions including GMP and Reimbursement applications.
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- Nihat Ozen    Consultant
© 2016. nihatozen.All rights reserved.
REGULATORY
eCTD Application
Pricing
Pharmacoeconomics
REIMBURSEMENT
GMP
- Umut Gumusbas    Consultant
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ANKofis Danısmanlık Ltd. Ataturk Bulvari, 167/13 06680 Kavaklidere / ANKARA / Türkiye +90 312 417 4071 / +90 312 418 8752 +90 312 417 40 72 www.ankofis.com.tr
For Regulatory Affairs: Mr. Umut GUMUSBAS                 umut.gumusbas@ankofis.com.tr   For Intellectual Property: Mrs.Ebru GUMUSBAS               ebru.gumusbas@ankofis.com.tr For Business Development: Mr. Nihat OZEN             nihat.ozen@ankofis.com.tr
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