DLRC Regulatory Consultancy Email Formats
Business Consulting and Services • 
Letchworth, England, United Kingdom • 101-200 Employees
DLRC Regulatory Consultancy Email Formats
DLRC Regulatory Consultancy uses 4 email formats. The most common is {first name}.{last name} (e.g., john.doe@dlrcgroup.com), used 70.8% of the time.
| Format | Example | Percentage |
|---|---|---|
{first name}.{last name} | john.doe@dlrcgroup.com | 70.8% |
{first initial}.{last name} | j.doe@dlrcgroup.com | 27.8% |
{first initial} | j@dlrc.co.uk | 1.4% |
Key Contacts at DLRC Regulatory Consultancy
Maggie Rahman
Associate Director, Senior Regulatory Consultant
Kadi Kuuskmae-Perry
Senior Regulatory Consultant - Associate Director
Michelle Blake
Associate Director And Senior Regulatory Consultant
Company overview
| Headquarters | Suite 201, The Nexus Building, Broadway,, Letchworth Garden City, Herts SG6 3TA, GB |
| Phone number | +441462372472 |
| Websites | |
| NAICS | 5416 |
| Keywords | Drug Development, FDA, Regulatory Affairs, MRP, DCP, Ectd, Scientific Advice, Regulatory Strategy, IND, EMA, Marketing Authorisation Applications, Centralised Procedure, Clinical Trial Applications, Maa'S, Nda'S, Orphan Drug Designations, Paediatric Investigation Plans (Pip)S, Pharmaceutical Regulations, Regulatory Complaince |
| Founded | 2005 |
| Employees | 101-200 |
| Socials |
About DLRC Regulatory Consultancy
The pathway to market is complex, but DLRC can simplify your journey. Operating from our UK, Germany, and US offices with over 1,000 years of combined experience, we collaborate with diverse clients, from top-five pharma companies to SMEs and start-ups. We develop and execute innovative phase-appropriate regulatory strategies to provide comprehensive support from very early in a product's lifecycle to post-licensing activities for medicinal products and medical devices. Our team comprises consultant experts in non-clinical, CMC, clinical, and MedTech fields from pharmaceutical, medical device, and regulatory agency backgrounds. With a wealth of knowledge and experience, we have proudly served over 130 companies of all sizes and backgrounds in various regulatory jurisdictions. Our service offering includes: Strategy • Global strategic advice • Regulatory route to clinic/market • Gap analysis & due diligence • EU CTR: Implementation & transition planning • Health authority engagement & negotiations • Expedited pathways • Paediatric development Operations • Procedural management: Global regulatory agencies • Clinical trial applications • Marketing authorisation • Medical and scientific writing • Regulatory operations and publishing • Regulatory lifecycle management Representation • US agent • Authorised representative medical devices • Legal representative under EU CTR • SME / ODD / MAH holder Our unwavering commitment to excellence has earned numerous accolades and industry recognition, solidifying our reputation as a trusted name in the life science industry. These include King’s Award for Enterprise in International Trade, TOPRA Awards for Regulatory Excellence, ISO 9001 Accreditation, Investors in People Silver Award, Cyber Essentials accreditation, and Queen’s Award for Enterprise in International Trade. Speak to us today to find out how our award-winning team can maximise the potential of your company and products.
Employees by Management Level
Total employees: 101-200
Seniority
Employees
Employees by Department
DLRC Regulatory Consultancy has 78 employees across 8 departments.
Departments
Number of employees
Funding Data
DLRC Regulatory Consultancy has never raised funding before.
DLRC Regulatory Consultancy Tech Stack
Discover the technologies and tools that power DLRC Regulatory Consultancy's digital infrastructure, from frameworks to analytics platforms.
JavaScript libraries
Security
Miscellaneous
JavaScript libraries
Analytics
Maps
JavaScript libraries
CDN
SEO
JavaScript libraries
Programming languages
Ireland
Spain
Frequently asked questions
4.8
40,000 users
