Specialty Medicines Market Access Patient Safety
PRODUCT QUALITY • COMPLAINT HANDLING

Product Quality Complaint

Report a suspected product quality issue to EndoCare+ for appropriate assessment, documentation, and follow-up.

WHAT SHOULD BE REPORTED HERE?

Reporting Channels

This channel is intended for suspected quality defects or concerns involving EndoCare+ products, including product appearance, packaging, labeling, container integrity, suspected damage, storage-related concerns, or other issues that may affect product quality.

Product Quality Complaint

Suspected defects, damaged packaging, labeling concerns, product appearance, container integrity, storage concerns, or other product quality issues.

Report a Quality Complaint

Adverse Event / Safety Report

If a patient has experienced a suspected adverse reaction or other safety-related event associated with a medicine, please use our Pharmacovigilance reporting channel.

Report an Adverse Event
Product Quality
Product Defect
Packaging / Label
Storage / Handling

Product Quality Contact

For questions regarding product quality complaints or supporting information, please contact EndoCare+ through the available reporting channel.


Contact EndoCare+

Important Safety Notice

If a product quality concern is associated with an immediate medical emergency or suspected serious adverse event, seek appropriate medical care immediately and submit the event through the Pharmacovigilance reporting channel.

Report an Adverse Event

For serious or urgent safety events, use the Pharmacovigilance emergency contact:

+967 784 444 699
QUALITY COMPLAINT FORM

Submit a Product Quality Complaint

Product Information

Quality Concern

Damaged packaging
Broken / leaking container
Missing or damaged seal
Labeling issue
Missing or incorrect information
Product appearance / physical change
Color / odor / texture change
Foreign particles / contamination
Tablet / capsule defect
Liquid / solution abnormality
Suspected temperature excursion
Missing / damaged components
Quantity discrepancy
Suspected counterfeit / falsified product
Other

Description of the Complaint

Storage & Handling Information

Supporting Information

Important: Where possible, please retain the affected product, packaging, labels, and batch information until further guidance is provided.

Reporter Information

PROCESS

What Happens After You Submit?

01

Report Received

Your submitted information is received through the designated reporting channel.

02

Case Documentation

Relevant information is documented for appropriate assessment and follow-up.

03

Quality Assessment

The reported concern is reviewed according to the applicable internal quality procedures.

04

Further Information

EndoCare+ may contact the reporter if additional information is required.

Preserve the Product Where Possible

If practical and safe to do so, please retain the affected product, packaging, labeling, batch information, and any relevant photographs until further guidance is provided.

TRACEABILITY

Quality Complaints & Product Traceability

Product quality information may contribute to appropriate quality assessment, traceability activities, and, where warranted, further quality or regulatory actions in accordance with applicable procedures.

Quality Complaint Handling

EndoCare+ maintains documented procedures for receiving, documenting, assessing, and appropriately following up on product quality complaints. Reported information is handled within the applicable quality and regulatory framework.

Need Help?

If you have questions about our quality complaint process or need assistance, our team is available to help.

Contact EndoCare+