GMP Compliance Consultingfor Pharmaceutical &Nutraceutical Manufacturers
GMP compliance without the guesswork.
Facility setup, formulation development and equipment solutions - specified, installed and validated to current FDA cGMP guidelines. Based in Ronkonkoma, New York, serving Long Island, New York and clients nationwide.
Enquiries answered directly by Mohammed Z. Rahman, GMP Auditor
Practice areas
05- 01Facility Setup & Compliance
- 02Formulation Development
- 03Equipment Solutions
- 04Custom Packaging
- 05New Business Development
Ronkonkoma, New York · Suffolk County & Nassau County
Credentials and practice scope
Engagements are led directly by Mohammed Z. Rahman, GMP Auditor and President - not delegated.
- 5
- Service disciplines
- Setup to maintenance
- 2
- Industries served
- Pharma & nutraceutical
- 1
- Point of contact
- GMP Auditor led
- FDA / cGMP
- Design and documentation standard
Five disciplines, one point of contact
Facility, formulation, equipment, packaging and market entry - handled by the same practice, so nothing falls between vendors.
Facility design and SOP systems built to FDA cGMP guidelines from day one.
View detailSolid dose, powder and coating formulation from bench through scale-up.
View detailSourcing, installation, in-process equipment, validation and preventive maintenance.
View detailPackaging solutions specified for the finished product and its line.
View detailStartup support for companies entering pharma or nutraceutical manufacturing.
View detail- Start a conversation
Not sure where to start?
Describe the facility or the product. We'll tell you what it actually takes.
A specialist practice, not a general engineering firm
Pharma and nutraceutical manufacturing is the whole business. That changes what you get.
- 01Direct GMP Auditor oversight
- The work is led by a certified GMP Auditor, not delegated to a junior engineer. Compliance risk is assessed by someone who has sat on the audit side of the table.
- 02Hands-on facility and equipment experience
- Specification, installation and commissioning are done by people who have physically stood the equipment up - so the design accounts for how it actually gets built.
- 03One point of contact, setup through maintenance
- Facility design, formulation, equipment and ongoing preventive maintenance run through a single relationship. No handoff gaps between vendors.
- 04Specialist scope, not general engineering
- Pharma and nutraceutical manufacturing is the entire practice. There is no general-contracting division that treats cGMP as an edge case.
Two verticals, two different problems
The manufacturing discipline is shared. The regulatory pressure and the pace are not.
Pharmaceutical Manufacturing
When the compliance stakes are absolute.
- FDA audit readiness
- Equipment validation
- Documented SOPs
Nutraceutical Manufacturing
Faster cycles, same manufacturing discipline.
- Small-batch to production
- Formulation flexibility
- Bringing production in-house
Free initial consultation
Ready to get your facility inspection-ready?
Talk to a GMP Auditor about your facility, formulation or equipment. No sales call first - the technical conversation is the first conversation.