Who We Are
We offer a full range of services extending from consulting, programming, basic and detail design, and project and construction management to the delivery of turnkey solutions.
About HauHet plc.
HauHet plc. Created in 2023 by Dimitrios N. Giannopulos, we are a team with passion for what we do with great professionalism, we belong to the field of medicines, cosmetics.
Our team consists of Pharmacists, Chemical Engineers, Mechanical Engineers, Biologists, Dermatologists and Architects. Everyone is personally involved in their part and in the direct service of our customers.
We help any company and business to manufacture, create, develop pharmaceutical and cosmetic products with prestige and reliability.
We cooperate with over 10 companies in Europe (Greece, Switzerland, Poland, Romania, Germany, Latvia, Estonia, France).
REGULATORY AFFAIRS & COMPLIANCE
– Formula Review and Change Control
– Cosmetic Product Safety Report (CPSR)
– Notification to EU authorities (Cosmetic Product Notification Portal – CPNP)
– Labelling compliance and translation (artwork and proofreading services)
– Period After Opening (PAO) assessment
– Cosmetic claims substantiation
– Cosmetovigilance (post-market surveillance)
QUALITY ASSURANCE
– Compliance with Good Manufacturing Practices (GMP)
DESIGN AND CONSTRUCTION OF GMP CLEAN ROOM
Planning
Feasibility Studies
Site Evaluations
Technical Concept
Project Management
Procurement
EPC/EPCM
Commissioning
Engineering
Business Integrated Modelling
Installation Planning
Approval Engineering
Installation
Technical Maintenance
Expert Leasing
Training
REGULATORY AFFAIRS AND REGISTRATION SERVICES
We offer wide range of regulatory affairs services as per our customer needs:
* registration of pharmaceutical products
* preparation and submission of registartion dossiers
* preparation and submission of pricing applications
* advisory services about local regulatory requirements
CONTRACT DEVELOPMENT SERVICES
HauHet plc. together with its contract development partners offers services of the whole process of a new Pharmaceutical product development from the sourcing of raw materials until the registration dossier preparation.
BΙΟΕQUIVALENCE STUDIES
- Protocol design
- Clinical phase
- Analytical methodology development and determination of the active compounds in biological fluids
- Validated assay methods
- Determination of pharmacokinetic parameters
- Statistical programming and analysis
- Bioanalytical, pharmacokinetics and biometrics study reporting/writing and full dossier preparation
e-Liquid
ORIGINAL RECIPE DESIGN
HauHet plc. helps its customers design original e-liquid and concentrated flavour ranges.
We work together with our customers to design bespoke compositions, from the simplest to the most complex flavours.
MANUFACTURING AND PACKAGING
HauHet plc. makes its widely-recognised know-how available to vaping industry professionals. We provide turnkey production, packaging and labelling services to suit all needs through our in-house expertise and industrial facilities that meet the strictest standards.
VAPE PRODUCT COMPLIANCE
TPD regulations and notification, labelling and CLP compliance, Safety Data Sheet (SDS) drafting and INRS declarations, etc. HauHet walks its customers through every stage of the e-liquid compliance process before shipping to market.
PRODUCT COMPLIANCE
- TPD DECLARATIONS
- MSDS (Material Safety Data Sheet)
- INRS DECLARATION
Headquarters
HauHet plc. – Xolo Go OÜ
Private Limited Company
Kalasadama 4
10415– Tallinn
Estonia
Email: hello@hauhet.co
Tallinn Trade and Companies Register – Reg. no: 14717109
EU VAT No.: EE102156920