Tergrig fze llc
LEGAL SUPPORT IN HEALTHCARE AND PHARMACEUTICALS

TERGRIG FZE LLC provides full legal support to players in the pharmaceutical market including international manufacturers distributors and pharmacy chains
ADVANTAGES
Deep industry expertise and a flexible approach to legal support in highly regulated sectors
QUALITY
We support both global pharmaceutical corporations and mid-sized wholesale businesses with tailored legal services
SUPPORT
We assist with product development and market entry for cosmetics and perfumes including formula patenting and trademark registration
EXPERTISE
We provide legal analysis translations and practical commentary on changes in Good Manufacturing Practice (GMP) and develop solutions aligned with industry specifics and regulatory requirements
WE OPERATE IN FULL COMPLIANCE WITH GXP STANDARDS
We audit production sites draft exclusive contracts and handle negotiations for raw material procurement and product manufacturing
trusted by industry leaders
Individual
entrepreneurs
Suppliers of medical devices and reagents
Pharmaceutical manufacturers and distributors
Drug developers (RND)
Pharmaceutical companies
Manufacturers and distributors of cosmetic products
Interaction with government authorities
/2
/6
Negotiations and legal representation
Corporate procedures and audits
/5
Support for business operations and contract management
/10
/9
Compliance with advertising regulations
/8
Procurement law compliance
/7
Registration distribution and circulation of medicines and medical devices
/4
Intellectual property rights protectionЗащиту прав интеллектуальной собственности
Legislative work and drafting of regulatory acts
/3
/1
Antitrust regulation
OUR TEAM PROVIDES SUPPORT ON ALL KEY LEGAL REGULATORY ISSUES INCLUDING


COSMETICS AND SUPPLEMENTS MARKET
TERGRIG FZE LLC successfully supports cosmetics and perfume manufacturers entering the EAEU market
WHY COSMETICS COMPANIES
CHOOSE TO WORK WITH US?
We inspect the production site draft exclusive contracts and manage negotiations for raw material sourcing and product manufacturing
RELIABLE AND SECURE MARKET ENTRY
We provide legal support to both major international pharmaceutical corporations and small to mid-sized wholesale companies
PRODUCT LABELING AND DESCRIPTION
We handle the full documentation package validate product composition and packaging and ensure seamless labeling compliance including DataMatrix and Chestny ZNAK systems
LEGAL PROTECTION AND CONFIDENCE
We represent your interests during inspections disputes and on marketplaces preventing bans fines and reputational risks
Legal support for product market entry
We manage import certification and trademark registration processes verify product composition and packaging for compliance and prepare documentation for labeling and online sales
Deep knowledge of the pharmaceutical industry and EAEU law
Our expertise is built on
Understanding the specifics of legal enforcement in the healthcare sector
We deliver practical effective and timely solutions tailored to your business needs with a focus on cost-efficiency and measurable results
A personalized approach to each client
Use of modern technologies in our practice
COMPETENCIES
The company provides support on all key legal and regulatory matters including
  • ANTITRUST COMPLIANCE
    We advise on antitrust regulations including representation in cases before the Russian Federal Antimonopoly Service (FAS)
  • LEGISLATIVE INITIATIVES
    We draft and promote legislative proposals and participate in working groups and public consultations
  • NEGOTIATIONS AND LITIGATION
    We represent clients in court government bodies and during negotiations and dispute resolution
  • GOVERNMENT RELATIONS (GR)
    We build effective communication with authorities and support participation in public procedures
  • CORPORATE PROCEDURES AND AUDIT
    We conduct legal audits support transactions manage corporate changes documentation and risk mitigation
  • PRODUCT REGISTRATION
    We provide full support for product registration procedures including communication with relevant regulatory bodies
We actively contribute to research and analysis in pharmaceutical regulation collaborating with leading academic and expert platforms including the EEC EMA FDA MGIMO University of the Russian Ministry of Foreign Affairs and the Federal State Institution GILS and NP.

We organize training sessions and practical workshops for industry professionals and publish analytical materials and articles in specialized media outlets.