Production and
R&D
Our products are manufactured in GMP Certified Pharmaceutical
plant. Our formulations are in the form of a) Capsules,
b) Tablets, c) Liquids, d) Ointments which are having
FDA licence and registration under Ayurvedic Medicines.
We are manufacturing high quality standard products
by using purified and highly standardized herbal extracts.
These extracts are total aqueous extracts in the form
of -
We are using this paste form extracts for our Liquid
(Syrup) products and Ointment (Cream) products.
R&D Center
In this era of globalisation where the Western Countries
are now opening channels to accept Ayurvedic drugs and
formulations as a main line treatment, our foundation
aims at being the front runner from the Indian Ayurvedic
Industry by taking initiative to develop a state of
art, internationally recognised R&D Center, along
with Herbal plants nursery.
We are developing a well equipped international standard
R&D Center at B-114, Addl. Ambernath MIDC, Dist-Thane,
Maharashtra. In lieu of the new policies laid down by
the Govt. of India which validate the requirement and
development of such a unique independent R&D Center,
we need to set up our own R&D facility. This will
enable us to establish clinical and laboratory data
validation which is the needs of today’s global
standards.
In our R&D Center we undertake the full spectrum
of preclinical safety and efficacy studies for Pharmaceuticals,
Biologicals and Nutracenticals. We undertake –
A) Quality Development Services
by the way of –
1. Nutritional Testing,
2. Active ingredient method development and Testing,
3. Formulation Development and Stability,
4. Improving actives release or bioavailbility,
5. Taste enhancing or masking,
6. Impurity Testing i.e. Heavy metals, pesticides, microbial
and Aflotoxin.
B) Formulation Development
–
1. Preformulation and formulation feasibility and Compatibility.
2. Active ingredient characterisation.
3. Pilot batch production.
4. Stability testing.
5. Validation and Regulatory Documentation.
C) Analytical Testing and Development –
Analytical testing and development is carried out with
highly competent analytical instrument.
1. Gas Chromatography (GC) with detectors (FID / ECD),
2. High performance liquid chromatography (HPLC).
3. UV-Visible spectroscopy (UV-VIS),
4. Mass spectrometry (MS),
5. Atomic absorption Spectrophotometry (AAS),
6. Fourier Transform Infra Red Spectroscopy (FTIR),
7. Nuclear Magnetic Resonance Spectroscopy (NMR),
8. Differentiate Scanning Colorimetry (DSC),
9. Thermogravimetry Analysis (TGA),
10. X-Ray Diffraction (XRD).
D) Toxicology Facility –
We have GLP and Non-GLP toxicity testing facilities
with validation and maintenance which is of international
regulatory standards.
