Takeda India | Leading Innovative Healthcare Solutions
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Great Place to Work
We are proud to be certified as a great workplace in India in 2022 and 2023 by Great Place to Work® Institute.
Top Employer
Certified as a Top Employer by the Top Employer Institute for three consecutive years in 2021, 2022 and 2023.
Most Preferred Workplace Award in Health and Wellness
We have received the Most Preferred Workplace Award in Health and Wellness for 2022-23 by Teams Marksmen
Notice
It has been brought to our attention that certain unscrupulous elements are sending out false communication claiming to be on behalf of Zydus Takeda Healthcare Pvt. Ltd. The communications are falsely stated to be from Zydus Takeda either by using Zydus Takeda / Takeda Logo or fake email IDs of company officials.
Please note that under no circumstances will Zydus Takeda ask potential employees (either directly or through a third party) to pay a fee, deposit, service charge, or other recruitment charges linked to securing a job at any stage of the recruitment process.
Zydus Takeda Healthcare Pvt. Ltd. and its affiliate companies bear no responsibility for amounts being deposited / paid in response to such occurrences.
What we do
Zydus Takeda
Patient Services
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Takeda Biopharmaceuticals India Private Limited
Zydus Takeda
CIN – U24231MH1999PTC119171
Medical Information (Intended for Health Care Professionals Only)
Media queries
Quality
Should be reported to Takeda within 01 business day
What is Pharmacovigilance?
Pharmacovigilance is the science and activities relating to the detection, assessment, understanding and prevention of adverse effects or any other drug-related problems with the ultimate goal of ensuring and improving patient safety.
What is an adverse event?
An Adverse Event (AE) means “any untoward medical occurrence in a patient or clinical trial subject administered a medicinal product and which does not necessarily have a causal relationship with this treatment.”
AE Reporting
- Anyone, including the public, who needs to report an adverse event can fill out the AE reporting form available at https://ae-reporting.com/ or by scanning the QR code.
- Adverse event reporting can also be done by sending an email with the following information to [email protected]:
- Details of product information
- Adverse event
- Reporter information
- Patient information (patient initials only, gender and age or age group).
- You can also directly call the adverse event reporting helpline at +91-9599959221 (available on all Working Days 9:00 AM to 5:30 PM).