Dietary supplements
From product idea to dietary supplement development, contract manufacturing, and successful FDA/ EU approval, and marketing of your dietary supplement
Pharma Expertise Consulting helps you to develop, manufacture and market dietary supplements in accordance with FD&C Act, FDA DSHEA, CFR 21 Part 101, EFSA, EU Health Claim Regulation and the Directive 2002/46/EC.
Pharma Expertise Consulting accompanies your dietary supplements throughout the entire life cycle (maintenance).
Depending on your needs, We are by your side through the whole product life cycle or can also implement singular steps such as designing advertising brochures, developing sales concepts, and brand strategies.
Marketing & Distribution
From product launch, medical marketing, FDA DSHEA health claims, social media marketing, trademark applications to efficient distribution channels and international sales network .
Regulatory Affairs
Pharma Expertise Consulting helps you with FDA dietary supplement approval in compliance with FD&C Act, DSHEA and for the EU-market persuant to EFSA & Directive 2002/46/EC.
Labeling & Mandatory Information
Pharma Expertise Consulting implements the labeling of your dietary supplements in compliance with the FDA CFR 21 Part 101, DSHEA and for the EU market with EFSA EU Health Claim Regulation .
Pharmaceutical development
We accompany you from the development of your dietary supplement in our laboratory (formulation, dosage form) to quality testing and manufacturing.
Analytics
We perform analysis and quality control of your dietary supplements according to FDA DSHEA, CFR 21 Part 101, EU Directive 2002/46/EC with HPLC, TLC, UV/VIS, GC.
In- & Outlicensing
Expand your product portfolio with dietary supplement licenses, private labels, developments, distribution rights & acquisitions.
Import & Export
We enable efficient import and export of dietary supplements with fulfillment of US and international customs and regulatory requirements.