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Projects
Clinical Research *
Clinical Reporting
Product Development
Real World Data Research
Study Operations & Management
Trial Design & Planning
Commercialization *
Brand Planning & Activation
Customer Engagement
Finance & Investment *
Financial Services
Investment Banking
Market Access & Policy *
Global Market Access
Government Policy
Medical Affairs *
Evidence Generation
Scientific Communications Development
Strategic Communications Planning
Strategic Stakeholder Engagement
Pharmacovigilance *
Risk Management
Safety Systems
Quality & Mfg *
Facilities & Equipment
Production & Supply Chain
Quality Management
Testing & Release
Regulatory *
Compliance
Labeling & Promotions
Maintenance & Renewals
Transparency & Disclosure
Technology & Operations *
Automation & Efficiency
Data & Analytics
Digital Health Solutions
Early Development
Informatics Infrastructure
Operations
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About
2005
Broadway Letchworth, Broadway, Letchworth, Hertfordshire, England, SG6 3, GBR
Overview
Strategic Regulatory Expertise for the Life Sciences
DLRC collaborate with diverse clients, from Top 5 Pharma companies to SMEs and start-ups. They develop and execute innovative phase-appropriate regulatory strategies to provide comprehensive support from very early in the lifecycle of a product right through to post-licensing activities for both medicinal products and medical devices.
Their team comprises consultant experts in non-clinical, CMC, clinical, and MedTech fields from pharmaceutical, medical device, and regulatory agency backgrounds. With a collective wealth of knowledge and experience, DLRC has proudly served over 130 companies of all sizes and backgrounds in various regulatory jurisdictions. Their partnership has enabled companies to achieve success in both their strategic and operational development objectives.
DLRC's hallmark is extensive expertise, agility and integrity. They are a global team motivated by solving complex challenges and excel in interactions with clients and regulators. Their flexible and efficient working approach means they can deliver for their clients, whether it be agile, standalone solutions or end-to-end regulatory outsourcing solutions.
DLRC’s unwavering commitment to excellence has earned numerous accolades and industry recognition, solidifying its reputation as a trusted name in the life science industry.
Strategic Regulatory Expertise for the Life Sciences
DLRC collaborate with diverse clients, from Top 5 Pharma companies to SMEs and start-ups. They develop and execute innovative phase-appropriate regulatory strategies to provide comprehensive support from very early in the lifecycle of a product right through to post-licensing activities for both medicinal products and medical devices.
Their team comprises consultant experts in non-clinical, CMC, clinical, and MedTech fields from pharmaceutical, medical device, and regulatory agency backgrounds. With a collective wealth of knowledge and experience, DLRC has proudly served over 130 companies of all sizes and backgrounds in various regulatory jurisdictions. Their partnership has enabled companies to achieve success in both their strategic and operational development objectives.
DLRC's hallmark is extensive expertise, agility and integrity. They are a global team motivated by solving complex challenges and excel in interactions with clients and regulators. Their flexible and efficient working approach means they can deliver for their clients, whether it be agile, standalone solutions or end-to-end regulatory outsourcing solutions.
DLRC’s unwavering commitment to excellence has earned numerous accolades and industry recognition, solidifying its reputation as a trusted name in the life science industry.
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Contacts
James Biddlecombe
Business Transformation Manager & Clinical Trial Regulation (CTR) Lead
Locations
Broadway Letchworth, Broadway, Letchworth, Hertfordshire, England, SG6 3, GBR
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James B. , Business Transformation Manager & Clinical Trial Regulation (CTR) Lead
DLRC
59 days ago