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Clinical Development
Global Clinical Operations
Project Management
Global Regulatory
Regulatory Services
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Biostatistics
Global Pharmacovigilance
Medical Information Solutions
ICSR & Literature Support
Medical Safety (Aggregate, Signal, Risk Management)
PSMF & Global QPPV Solutions
Clinical Safety & AE/SAE Management Solutions
MedTech Safety
Quality Assurance
Good Clinical Practice (GCP)
Good Pharmacovigilance Practice (GVP)
Our Expertise
Therapy Areas
Specialties
Softwares
aRMM TREx
Insights & Resources
Blogs & Whitepapers
Case Studies
Brochures & Flyers
Webinars & Podcasts
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Event Insights
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Contact Us
For Business Enquiries
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Insights & Resources
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Insights & Resources
Clinical Trials
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Quality Assurance
Blog
The Evolution of PRO Collection: From Paper Diaries to ePRO Systems
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Transforming Complexity into Success: A Large-Scale Global Phase III Biosimilar Dermatology Trial
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Flyer
Biometrics
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Flyer
Clinical Services
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Flyer
CT Quality Assurance
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Flyer
Medical Affairs
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Article
Pulmonary Disease Introduction: Prevalence, Causes, Prevention & Treatment
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Blog
Strategic Planning for Patient Recruitment
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EMA
FDA
MHRA
Product Management Service (PMS) public API beta release - Technical overview and live demo, Online, from 13 July 2026, 14:00 (CEST) to 13 July 2026, 15:30 (CEST)
Source: EMA
Published on 2026-09-01
Managing product data quality in PMS: processes, known issues, current status and best practices, Online, from 21 July 2026, 14:00 (CEST) to 21 July 2026, 15:30 (CEST)
Source: EMA
Published on 2026-09-01
Human medicines European public assessment report (EPAR): Myqorzo, aficamten, Date of authorisation: 12/02/2026, Revision: 2, Status: Authorised
Source: EMA
Published on 2026-09-01
Human medicines European public assessment report (EPAR): Omvoh, mirikizumab, Date of authorisation: 26/05/2023, Revision: 9, Status: Authorised
Source: EMA
Published on 2026-09-01
ACT EU multi-stakeholder platform annual meeting, Online, European Medicines Agency, Amsterdam, the Netherlands, Broadcast, 22 October 2026
Source: EMA
Published on 2026-09-01
Voluntary data submission pilot to advance innovative alternatives to animal testing
Source: EMA
Published on 2026-09-01
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FDA approves pembrolizumab for adenocarcinoma
Source: FDA
Published on 2025-04-08
Approved Drug Products with Therapeutic Equivalence Evaluations (Orang
Source: FDA
Published on 2025-04-08
Additions/Deletions for Prescription and OTC Drug Product Lists
Source: FDA
Published on 2025-04-08
Recalls small number of acne products for benzene contamination
Source: FDA
Published on 2025-04-08
FDA Drug Shortages
Source: FDA
Published on 2025-04-08
FDA Drug Shortages
Source: FDA
Published on 2025-04-08
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Cobalt-chrome modular neck hip replacements: risk of metal-wear effects and revision surgery (DSI/2026/010)
Source: MHRA
Published on 2026-08-26
MHRA Safety Roundup: August 2026
Source: MHRA
Published on 2026-08-25
NGPod pH testing device: quarantine and dispose of all devices (DSI/2026/009)
Source: MHRA
Published on 2026-08-24
Field Safety Notices: 17 to 21 August 2026
Source: MHRA
Published on 2026-08-24
Class 2 Medicines Recall: Zentiva Pharma UK Limited, Fingolimod Zentiva 0.5 mg Capsules, EL(26)A/37
Source: MHRA
Published on 2026-08-20
All rectal catheters (gas and colic relievers): Do not use in infants, including for the treatment of colic, gas-related discomfort or constipation (DSI/2026/008)
Source: MHRA
Published on 2026-08-18
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