Adverse Event Reporting
It is the company policy to ensure safety of medicinal products and medical devices manufactured by or on behalf of Merck by capturing, recording and assessing all the adverse events and incidents. Adverse events and incidents are monitored and reported to the management and to the relevant . Adverse event reporting is important so as to safe-guard a patient’s well-being and to identify less common adverse events that may not have been observed during clinical development. It is also a legal obligation, both Local and Global Regulatory Authorities, to report all the adverse events.
For adverse event reporting with respect to pharmaceutical products of Merck Limited or Merck Specialities Private Limited, kindly contact our local Drug Safety Unit.
Contact persons
Local Drug Safety Officer
Ms. Indira Nuthakki
Direct Line: +91 (0)22 6660 9030 / Mobile: +91 (0)9833256805
Fax: +91 22 24971563
Deputy Drug Safety Officer
Ms. Aparna Mirashi
Direct Line: +91 (0)22 66609064/ Mobile: +91 (0) 9769721208
Dr. Rajiv Rana
Direct Line: +91 (0)22 6660 9117 / Mobile: +91 (0)90046 76731
Direct Line: +91 (0)22 6660 9117 / Mobile: +91 (0)90046 76731
Address
Shiv Sagar Estate 'A'
Dr. Annie Besant Road
Worli, Mumbai 400018
Maharashtra, India
Shiv Sagar Estate 'A'
Dr. Annie Besant Road
Worli, Mumbai 400018
Maharashtra, India
