Max-Brom London Pharmaceutical Expertise
At Max-Brom London Pharmaceutical, we help pharmaceutical, biotechnology, and medical device companies bring life-changing therapies to market. From early development through clinical, regulatory approval, and commercialization, we provide expert guidance to navigate complex challenges and accelerate success. Our mission is simple - improving patient health and safety by delivering the highest quality regulatory, compliance, clinical research, pharmacovigilance, and medical information services throughout the entire product lifecycle. We work in close partnership with our clients, often as an extension of their teams, to improve the health and safety of patients. Our ability to be nimble, coupled with a passion for excellence, ensures our services exceed clients’ expectations. For over 25 years, Max-Brom London Pharmaceutical has evolved to support pharmaceutical, biotechnology, and medical device companies
at every stage of the product lifecycle. As we grow, our mission remains the same: delivering world-class solutions to help you bring innovative therapies to market with confidence.. Max-Brom London Pharmaceutical’s growth over the past two decades reflects our mission. We continue to expand our global impact, helping our clients bring safe, effective therapies to patients who need them.
Sustainability Starts with Our Core Principles
We foster a culture of respect, inclusion, and opportunity to enable employee well-being, professional growth, and a culture of belonging.
Dedicated DEI program and leadership
Risk inventory assessments
Volunteer and flexible time off
Wellness benefits, annual programming, and challenges
Employee Resource Groups and clubs
Feedback and upward mobility
Charity match programs
Talent acquisition and retention
Mentorship programs
Training and continuous education opportunities
And more!
Ethical Leadership
We uphold integrity, transparency, and accountability in all aspects of our business, ensuring responsible decision-making, data privacy, and compliance with global standards.
Advanced Data Security and Privacy Programs
Compliance with labor laws within each operating region
Quarterly Board Reporting on Sustainability Program
Transparent and accessible leadership through Town Halls.
Max-Brom London Pharmaceutical aims to help your business succeed by working to streamline the pharma/biotech/medical device regulatory process. Our experienced team of regulatory consulting and compliance experts commands an unparalleled breadth and depth of knowledge pertaining to the US and European regulatory frameworks and can work with you to accomplish your business objectives. Using our deep scientific knowledge combined with our significant regulatory experience, our Regulatory Sciences team develops and executes detailed strategies for your product, providing a clear path forward through all the critical milestones to help you achieve a successful outcome with the regulators.
Comprehensive Medical Information and Contact Center Services
With strategically positioned and seamlessly integrated contact centers around the world, we provide customizable medical information services to meet the needs of companies of all sizes. Whether you need medical information, patient support, commercial inquiry handling, or other extended medical information services, our team of medical information specialists have the knowledge and experience to effectively support your needs.Max-Brom London Pharmaceutical has more than 25 years of expertise in delivering Medical Information services to our clientele. We specialize in distributing vital information regarding our clients' healthcare products to healthcare professionals, patients, and the wider public. Our dedicated team consists of seasoned healthcare professionals (HCPs) and graduates in life sciences who function as an integral part of your team, facilitating the exchange of clinical and scientific information related to drugs and devices, as well as product safety.
Data Integrity
Data without integrity puts patients at risk. Data Integrity is a "hot topic" because many of the controls implemented decades ago for paper records, have not yet been implemented for electronic records and computer systems in spite of recent guidelines from the FDA, EMA, MHRA, PIC/S, and WHO. Our experts have experience applying the ALCOA principles to real-life scenarios to minimize data integrity risks through remediation of systems, policies, procedures, and data governance programs.
Max-Brom London Pharmaceutical specializes in solving complex challenges. Our experienced compliance consulting professionals will seamlessly integrate with your team to do more than simply identify potential risks. We provide recommendations to mitigate those risks and will work side-by-side with you to implement improvement plans and collaborate with your team in addressing those risks.
From early concept development through each clinical phase, product launch, and commercialization, our Quality and Compliance Consultants partner with clients around the world to help ensure regulatory expectations are met, such as compliance with DSCSA and EU FMD, business goals are achieved, and patient health and safety is assured and improved. We do this with an unwavering focus on delivering the highest quality services through our diverse team of qualified subject matter experts (SMEs).
DR.MICHAEL TREMBLAY, PharmD
Chief Executive Officer (CEO)
Leads the company’s vision, strategy, and overall operations, ensuring growth and innovation in pharmaceutical advancements.
PROF.MARTIN FRIEDRICH,PhD
Chief Scientific Officer (CSO)
Oversees research and development, driving cutting-edge drug discovery, biotechnology, and gene therapy innovations.
Our quality and service reliability rest on a unified system that spans development, manufacturing, and logistics. Max-Brom London Pharmaceutical has operated under EU GMP since 2008, holds ISO 9001:2015 certification for its Quality Management System, and now also maintains a Good Distribution Practice (GDP) licence for sourcing, warehousing, and outbound shipments. Together, these accreditations ensure that every stage—production, testing, and distribution—is in full alignment with global regulatory expectations, providing consistent, traceable quality for your drug-substance projects.