PharmaLex GmbH
About us
Needing a partner to launch products with confidence? Looking for an experienced service provider to bring the promise of your therapies to life? PharmaLex, a Cencora company, supports on the path to commercial success. Our services are aimed to deliver expertise to pharmaceutical and medical device companies throughout the product lifecycle. We navigate through the complex regulatory landscape and leverage our extensive knowledge and global presence to guide small and medium-sized companies through the complexities of product development and regulatory requirements. By offering scalable, tailored solutions, PharmaLex empowers companies to successfully bring innovative pharmaceutical and medical device products to market and thereby improving patient outcomes and advancing healthcare.
During early phase development PharmaLex, is often engaged to provide a holistic plan and the needed resources for executing essential support for compounds needed for life-saving therapies. Our focus is on viewing the entire product development cycle holistically. We not only consider the next step but also look to the future. We think about the critical endpoints of a study and what is required for the product to be approved by various regulatory authorities.
Our experts have experience in a wide range of therapeutic areas and across different regions worldwide. Our goal is to help the process flow seamlessly from one phase to the next. We partner with our clients to create value, rolling up our sleeves to solve challenges. Our team of subject matter experts provides hands-on support and expertise at every stage of the product development process. We believe in a collaborative approach, working closely with our clients to navigate the complexities of regulatory requirements and market demands.
As part of Cencora, a global leader in healthcare, we offer tailored services for the pharmaceutical, biotech, and medtech industries. From early strategic planning activities through clinical development to regulatory submission processes and post-market activities, we support our clients throughout the entire product lifecycle. Our experts leverage technology-driven solutions to ensure our clients’ needs are met, their reputation is protected, and their business goals are achieved.
At PharmaLex, we are passionate about making a difference in the lives of patients. We are driven by a commitment to excellence and a desire to help our clients succeed. Our team is constantly innovating and adapting to the ever-changing landscape of the pharmaceutical industry. We stay ahead of the curve by investing in the latest technologies and methodologies, ensuring that our clients benefit from cutting-edge solutions.
PharmaLex –Together, we bring your innovations, hard work, and aspirations to patients around the world.
At PharmaLex, we are passionate about making a difference in the lives of patients. We are driven by a commitment to excellence and a desire to help our clients succeed. Our team is constantly innovating and adapting to the ever-changing landscape of the pharmaceutical industry. We stay ahead of the curve by investing in the latest technologies and methodologies, ensuring that our clients benefit from cutting-edge solutions.
Address
Basler Str. 7
61352 Bad Homburg
Germany
E-mail: info@pharmalex.com
Phone: +49 621 181538-0
Internet: www.pharmalex.com/
Contact person:
Senior Business Development Manager Tim Heyeck
E-mail: tim.heyeck@pharmalex.com
Senior Director, Reg. Southern Europe, Service Solution Lead M&A Dr. Katharina Rönnpagel
E-mail: Katharina.Roennpagel@pharmalex.com
Products & Services
Regulatory Affairs: Assistance with navigating the regulatory landscape, including submissions to health authorities and compliance with regulations.
Pharmacovigilance: Services related to the monitoring of drug safety and the management of adverse event reporting.
Market Access: Support in gaining access to markets, including pricing strategies and reimbursement processes.
Clinical Development: Consulting services for clinical trial design, management, and regulatory submissions.
Quality Assurance: Ensuring compliance with quality standards and regulations throughout the product lifecycle.
Medical Affairs: Support for medical communications, scientific information, and stakeholder engagement.
Commercialization Services: Strategies and support for bringing products to market effectively.
Merger and Acquisition (M&A): Support for M&A activities, emphasizing a holistic approach that involves various stakeholders and functions, such as regulatory affairs, to ensure successful integration and achievement of goals like increasing market share, replenishing product pipelines, entering emerging markets, and reducing costs through consolidation.
Strategic and Scientific Consultancy: Tailored consulting services from a team of strategic and scientific experts, helping clients navigate complex hurdles in drug development and bringing new products to market, leveraging over 25 years of global expertise.