Our Services
Where Excellence Meets Compliance
Our diverse range of services encompasses bulk drug supply, clinical trial support, and cGMP manufacturing, prioritizing the dynamic needs of researchers, government agencies, and businesses alike.
As a registered DEA Schedule I (use roman numeral) Bulk Drug Manufacturer, Importer, and Distributor of Schedule II-V, controlled substances we provide global access to a varied array of pharmaceutical substances, supporting medical researchers and developers in their pursuit of botanical drug formulations.
With a focus on development and commercialization, we lead the way in introducing over-the-counter consumer-facing botanical products and prescription pharmaceuticals.
Manufacturing
Manufacturing
Schedule I Bulk Manufacturing
We are a Pharmaceutical Distributor of Schedule II-V controlled substances. This allows Royal Emerald to bulk manufacture botanical extracts and compounds, and distribute them to DEA-licensed researchers. This license is crucial for conducting extensive research and developing new drug formulations.
Our products are cultivated and manufactured following strict Good Manufacturing Practices (GMP) and Good Agricultural & Collection Practices (GACP) creating high-quality, and consistent products
Research
Research & Development
Our company stands at the forefront of innovation, offering dedicated Research and Development (R&D) support to researchers and universities engaged in diverse stages of clinical trials and botanical research worldwide. As a committed partner, we extend comprehensive trial sponsorships, fostering collaboration between academia and industry to accelerate the translation of groundbreaking research into tangible advancements.
Research
Compliance
Compliance
Compliance Support
Royal Emerald is here to provide regulatory and compliance assistance in the handling and research of Schedule I controlled substances.