Naturchem LLC facilitates the trade of Active Pharmaceutical Ingredients between drugmakers and distributors. Our API are a representation of the most renowned pharmaceutical manufacturers, making us trade nothing but the best.
We are able to bring active pharmaceutical ingredients to you anywhere in the world, and our commitment to quality ensures that you get the product you need in a timeframe you can count on.
Naturchem LLC’s Pharmaceuticals & Healthcare Regulatory Affairs team is a niche scientific and regulatory consulting group. We guide and assist pharmaceutical, biotech and healthcare companies in the design and implementation of innovative and global regulatory strategies in order to expedite product development and registration of drugs, biologics, medical devices, combination products, and other healthcare products for all stages of development.
Our professionals have expertise in the legal and regulatory environments, as well as in clinical research protocols. We collaborate with companies to bring products to the market in the most efficient and cost-effective manner, within an evolving and increasingly challenging regulatory environment.
Dossier preparation is an essential part of all drug development programs. Gathering the product information, clinical and manufacturing data regulatory agencies use to assess a drug is a complex process that involves multiple stakeholders.
The dossier production can be a costly process that can delay or even derail the drug development process. NaturChem LLC offers a comprehensive range of pharmaceutical dossier preparation services that streamline production of the registration file.
We gather data on the manufacturing process of a pharmaceutical product, the materials involved, their analysis, stability data, data on animal and human studies along with administrative documents in order to get a product registered.