Our R&D Capabilities - What We Can Do for You
Process Development
* Extraction process optimization - higher yields, better purity, more consistent active ingredient profiles
* Novel ingredient development and scale-up - from lab-scale feasibility to commercial production
* Yield and efficiency optimization - improving your cost-per-gram without touching specification
* Custom sample preparation - tailored to your formulation trials, delivered to your timeline
Quality & Analytical Support
* Method development and validation - analytical methods built to your regulatory market requirements
* Stability studies and shelf-life determination - documented to support your product registration and label claims
* Contaminant and residue testing - heavy metals, solvent residues, pesticides, microbiology
* Regulatory-compliant documentation - formatted for US, EU, and other major market submissions
Application Support
* Formulation recommendations - specific to your application, dosage form, and target consumer
* End-product troubleshooting - when your formula isn't performing as expected, we dig into why
* Industry trend analysis and application white papers - available to clients developing in emerging categories
* Collaborative new product development - for clients who want a co-development partner, not just a manufacturer
Our Dedicated R&D & Testing Center
In April 2025, we completed and launched our new independent R&D and testing center - a purpose-built facility representing a significant investment in our technical capabilities.
Equipped with HPLC, GC, UV-Vis, AAS, and a dedicated microbiology laboratory, the center operates as a fully independent unit - separate from production, focused entirely on development, validation, and client support.
What this means for you
* Faster custom sample turnaround - dedicated development capacity means your trial requests don't compete with production schedules
* Accelerated new product development - from initial feasibility to pilot batch, with full analytical documentation at every stage
* Expanded testing scope - in-house capability for the full analytical panel your regulatory submissions require, without reliance on third-party labs for routine testing
How We Partner with You
Every client engagement starts with a real technical conversation. Here's how we respond to the requests we hear most often:
|
Your Need |
Our Response |
|
"Can you develop an extract with this specific active profile?" |
We design and trial the extraction process, deliver characterized samples, and scale up once you're satisfied |
|
"We need stability data for our regulatory submission." |
We conduct, document, and deliver stability studies formatted to your target market requirements |
|
"Our formulation isn't performing as expected." |
We troubleshoot the root cause - whether it's particle size, solubility, compatibility, or something upstream |
|
"We want to explore a new ingredient category." |
We research the botanical landscape, develop a pilot formulation, and co-develop with you from there |
|
"Can you match a competitor's spec?" |
Send us the COA - we'll reverse-engineer the profile and develop a comparable or superior specification |
Start a Technical Conversation
Whether you have a detailed brief or just an early-stage idea, our R&D team is the right first call.
Reach out with your project background - ingredient category, target application, regulatory market, and any existing specifications - and we'll respond with a technical assessment within 48 hours.
