Merck Safety Reporting

You can report one or more Adverse Event(s) for each submission

(description to include Patient Identifier i.e. age or gender, Date of Awareness, Batch #, and Batch expiry date)
       Limit to 1500 characters. Do Not include URL links.
(optional field for you to enter your company's internal case reference ID, if available)
→ Upload the MEDWATCH/CIOMS Global Safety Intake Form or similar form(s) for reporting the Adverse Event.
→ Maximum upload size is 35MB
→ File format includes ZIP, PDF, DOCX, DOC, PPT, PPTX, XLS, XLXS, JPEG, JPG and PNG
→ Image requirement if reporting Product Quality issue:
      ○  6-sided photos of the product – with visible defect and batch details

The information provided concerning the reported event will be handled according to current worldwide regulatory requirement. Please read more about Our Company’s privacy commitment at https://www.msdprivacy.com/

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The adverse experience or product quality information you provide is shared with regulatory agencies, Merck subsidiaries worldwide, and business partners with whom we have contractual agreements. Any information that identifies the patient directly, such as the patient's initials or date of birth, will be handled confidentially and in line with Merck corporate policies and local regulations. You have a right of access to your personal data which we hold about you. For further details on Merck’s privacy policy, please visit: www.msdprivacy.com