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> Právní specializace > Life Sciences

Life Sciences

Life Sciences

Key contacts

Jaroslav Havel
Managing Partner
jaroslav.havel@havelpartners.cz

Václav Audes
Partner
vaclav.audes@havelpartners.cz

We have been focusing on the business and legal regulation of the pharmaceutical and health sectors (Life Sciences) for a long time now. Thanks to our specialised team comprising more than 10 lawyers, we are equipped with unique know-how, practical experience and detailed knowledge of market standards.

Our clients are leading global manufacturers of pharmaceuticals, medical devices, cosmetic products and food supplements, distributors, hospitals, clinics, private physicians, research institutes, laboratories, pharmacies, biotechnological companies, and other entities doing business in these fields or exercising state authority.

We advise our clients in individual pharmaceutical and health sector regulation areas and in other specialised areas closely related to them, particularly the area of personal data protection, public procurement, M&A, competition and IP/IT. When advising in these particular specialised areas, we draw on our extensive practical experience. Our services take into account all specifics of the pharmaceutical and health sectors.

We specifically focus on the following areas in the long run:

PHARMACEUTICAL LAW

  • Pharmaceuticals, medical devices, cosmetic prducts, food supplements
  • Market access agenda
    – Reimbursements from the public health insurance; price regulation
    – Agreements with health insurance companies (risk sharing)
    – Assessment and set-up of various distribution models (standard distribution, direct-to-hospital model, commission model, consignment warehouses)
  • Compliance agenda – interaction with health professionals and health service providers
    – Providing grants, sponsoring, cooperation with experts, patient organisations and professional organisations, educational events for professionals
    – Drafting contractual documentation
    – Assessments in terms of legal regulations and codes of ethics (AIFP, EFPIA, MedTech, etc.)
    – Transparency & disclosure
  • Business agreements
    – Distribution and logistics agreements
    – Bonus arrangements and related advisory
    – Market research agreements
    – Data purchase agreements
    – Register of contracts, trade secrets and related advisory
    – Electronic signatures
  • Regulatory matters
    – Regulation of production, import, distribution, provision and sale
    – Registration, notification and reporting with competent administrative authorities
    – Digitisation (mail order, home delivery, etc.)
    – Product labelling requirements
    – Withdrawal of products from the market
  • Advertising
    – Assessment of promotional materials, incl. TV spots
    – Educational campaigns
  • Clinical trials and medical affairs agenda
  • Clinical trial agreements
    – Patient’s informed consent
    – Ensuring treatment after termination of a clinical trial (post-trial access)
    – Specific treatment programmes (compassionate use)
    – Patient support programmes
  • Manufacturers’ liability and claims for the compensation of damage caused by medicine or other products
  • Representation in administrative and judicial proceedings (particularly before the State Institute for Drug Control, the Ministry of Health)
  • Drafting bills (e.g., in the area of medicines price policy)
  • Relationships with the non-profit sector

HEALTH LAW

  • Establishment and transformation of health service providers
  • Health service provision regulation – hospitals and clinics
  • Reimbursement from the public health insurance
  • Negotiating agreements with health insurers
  • Compliance programmes
  • Professional accountability and insurance
  • Rights and duties of patients, physicians and educational institutions
  • Telemedicine
  • Keeping health documentation, GDPR compliance

ADDICTIVE SUBSTANCES

  • Permission to handle addictive substances
  • Advice in the fields of production, distribution and sale of cannabis and cannabis products
  • Regulatory obligations related to the handling of addictive substances
  • Audits and comprehensive set-up of registers and handling of addictive substances at health service providers
  • Using cannabinoids and other substances in foodstuffs and other products

We also address all of the above topics in our professional publications, lectures and on our blog.

Publications and newsletters

Legislative changes in the field of medical devices
Authors: František Neuwirth, Denisa Fuchsová In December 2022 and January 2023, new legislation … read more »

Partners

  • Robert Nešpůrek
  • Václav Audes

Senior Associates

  • František Neuwirth
  • Kateřina Slavíková

Associates

  • Michal Blahovec
  • Denisa Fuchsová
  • Zuzana Hargašová
  • Lenka Ostró
  • Martin Rott

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Contact Us

OFFICE PRAGUE
Tel.: +420 255 000 111
Email: office@havelpartners.cz

OFFICE BRNO
Tel.: +420 545 423 420
Email: office@havelpartners.cz

OFFICE BRATISLAVA
Tel.: +421 232 113 900
Email: office@havelpartners.sk

OFFICE PILSEN
Tel.: +420 371 005 320
Email: office@havelpartners.cz

OFFICE OLOMOUC
Tel.: +420 581 000 310
Email: office@havelpartners.cz

OFFICE OSTRAVA
Tel.: +420 255 000 111
Email: office@havelpartners.cz

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