At Esmeray Law Office, we can help medical and healthcare professionals with a wide range of services tailored specifically to their needs.

We can assist on the following matters;

1-      Matters related to clinical trials

-          Negotiating, drafting and reviewing of clinical trial agreements, investigator agreements, agreements for research organisation,   

-          Advising on the regulatory issues of clinical trials, especially necessary authorisations from the competent authorities, committees.

2-      Matters related to co-marketing

-          Negotiating, drafting and reviewing of  co-marketing agreements, co-promotion agreements,

-          Advising on the regulatory requirements for contracts concerning joint sales activities

-          Advising on issues of antitrust law

-          Advising on liability issues.

3-      Matters related to manufacturing, supply and services

-          Negotiating, drafting and reviewing of manufacturing agreements, supply agreements, service agreements (consulting, logistics etc.), technical agreements,

-          Advising on the regulatory aspects of contract manufacturing and the outsourcing of other activities to third parties.

4-       Matters related to licensing and partnering

-          Negotiating, drafting and reviewing of licensing and partnering agreements, non-disclosure agreements, letter of intent and term sheets

-          Conducting due diligences   

-          Advising on antitrust law in licensing

-          Advising on regulatory aspects of contracts

-          Resolution of disputes arising from licensing and partnering agreements.

5-      Matters related to product liability

-          Defense or settlement of product liability claims regarding medicinal products or medical devices

-          Advising in connection with safety objections raised by regulatory authorities

-          Advising on the implementation of corrective action such as product recalls, additional safety instructions or temporary restrictions on use.

6-      Matters related to public procurement

-          Advising and acting for pharmaceutical companies and medical device manufacturers in public tenders,

-          Advising and acting for pharmaceutical companies and medical device manufacturer in review procedures,

-          Negotiating, drafting and reviewing of business partnership, consortium and sub-contracting agreements,

-          Advising on the preparation of tender documents.

7-      Regulatory

-          Advising on pharmaceutical and medical device laws

-          Advising on regulations relating to manufacturing, approval and distribution of medicinal products and medical devices,

-          Advising on regulations relating to data exclusivity,

-          Advising on regulations relating to intellectual property protection,

-          Advising on regulations relating to wholesale of medicinal products.

8-      Matters related to research and development

-          Negotiating, drafting and reviewing research and development agreements,

-          Advising on employee inventions.