ABOUT US

ALTA MEDICAL SERVICES is an emerging company based in Barcelona.

We are a specialized consulting firm on Medical Affairs, which provides a full range of customised guidance, advice, support, and solutions to health science companies along the whole life-cycle of new medicines, devices, and programs.

We are talented experts committed to supporting our clients in achieving a clear strategy pursued through effective and aligned activity.

We are passionate about our work, we employ strategic global thinking, and are able to provide customised innovative solutions focused on compliance from a medical perspective, as we have the judgment and expertise to interpret the codes and regulations under the increasing regulatory scrutiny that the industry is facing.

We help our clients to shift to a new paradigm of medical compliance and provide guidance on the risk evaluation of different medical and commercial activities, finding innovative solutions that deliver both value and a sustainable competitive advantage for each organisation.

Anna Muñoz

PhD MD is the founder and Managing Director of Alta Medical Services. Prior to starting this company, she held various management positions related to Global Medical Affairs in different large and medium-sized companies. In these different roles, she has gained the expertise, knowledge, and judgment to establish a company culture based on medical compliance. She is a Senior Global Medical Affairs Leader with extensive expertise in leading medical support of the marketed and late-stage development products and has significant ability in translating clinical data into strategic product medical plans. She has broad experience in compliance with medical affairs; working with high ethical standards. Extensive knowledge in increasing awareness & understanding, reviewing/ensuring the accuracy of relevant codes and standards applied to the development of global brand-specific related material and activities, and strong experience in medical writing of internal training, providing F2F deliverables, and supporting the medical information teams.

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Eulàlia Olesti

External senior consultant. Regulatory/scientific manager at the Clinical Pharmacology department of the Hospital Clínic de Barcelona. Experience on Advanced Therapy Medicinal Products (ATMPS) scientific and regulatory assessment with a broad experience in clinical academics (PhD). Passionate about science communication with a wide-range expertise developing effective pharmaceutical education. Strong scientific background in clinical pharmacology, recorded by more than 14 first authors publications in peer-review journals

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Àngel Ramírez

Scientific consultant

His enormous passion for science and his desire to improve global public health drove him to graduate in Biomedicine from the University of Barcelona, getting specialised in Advanced Microbiology. He counts with experience in four different laboratories where he has actively contributed to developing solutions that aim to improve people's quality of life. Throughout his education and experiences, he has cultivated solid scientific knowledge and strengthened skills to analyse and effectively communicate scientific information. He is currently pursuing a Master's degree in Clinical Trials and Medical Affairs, and aspires to leverage his expertise and abilities to contribute meaningfully to the healthcare industry.

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VISION

ALTA MEDICAL SERVICES provides guidance on how to transform the role of tactical enforcer of compliance functions into that of strategic advisor, encouraging a culture of ethics and integrity in every employee at each pharmaceutical company that requires our services.

We design pragmatic, efficient ways to:

- Drive companies to achieve an enterprise-wide awareness of compliance risk, reviewing the client’s approach to medical compliance.

- Build a company culture that allows compliance to be viewed as a source of competitive advantage and customer differentiation.

- Identify what can be done in to achieve compliance and to introduce the culture as part of the DNA of the company.

We are proud of what we do, ensuring:

- A correct interpretation of the relevant codes and standards that cover the different stages involved in the different phases of the drug/medical device lifecycle.

- An independent viewpoint and cover a great number of compliance services related to commercial and medical interaction.

- Innovative, efficient and pragmatic solutions with initiatives tailored to each specific project, adding value and giving your organisation a sustainable competitive advantage.

- Extremely accurate management across the different teams of the 'off-label use' prohibition required by regulators.

We act as an extension of the client, ensuring every single activity is delivered to exceptional standards and bringing commitment, integrity and pride to everything we do.