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Adverse Event Reporting

Global Medical Enquiries and Adverse Event Reporting

Specialist teams are available within BPL, and they can assist Healthcare Professionals with medical information or pharmacovigilance enquiries.

For medical information, please call +44 (0) 20 8957 2255 or Email: Medinfo@bpl.co.uk

Adverse events should be reported to BPL Medical Department on adr@bpl.co.uk or call
+44 (0) 20 8957 2622.

Opening hours:
Monday – Friday 09:00 -17:00 UK time

To report an adverse event outside these hours, please call +44 208 957 2200

Contact Address:
Bio Products Laboratory Ltd
Dagger Lane
Elstree
Herts
WD6 3BX
UK

Adverse events should also be reported to the National Competent Authority. The information for the UK, US and Germany can be found on this page.

UK: Adverse Event Reporting

Adverse events should be reported.  Reporting forms and information can be found at www.mhra.gov.uk/yellowcard.

Mexico: Medical Enquiries

Envíe informes de efectos secundarios a:

medinfo@phvlatam.com

Tel +52 5571 002 515

Germany: Adverse Event Reporting and Medical Enquiries

Nebenwirkdungsmeldungen richten senden Sie bitte an

bpl@medwiss-extern.de

FAX +49 (0) 2408 956 8072

Tel +49 (0) 2408 146 0245

US: Adverse Event Reporting and Medical Enquiries

To report an adverse event you think may be related to a BPL product, contact us at
844-4BPLUSA  (844-427-5872)

MedInfo@BPL-US.com

For general product, medical information or questions about reimbursement, contact us at
844-4BPLUSA  (844-427-5872)

MedInfo@BPL-US.com