Quality Assurance Protocol

Pharma Discipline in Everyday Nutrition

Every batch of Loginerve and Loginutra is manufactured under strict GMP compliance in India, validated for chemical identity, active potency, heavy metals, and microbiological safety.

GMP-Certified Facilities

Formulated in facilities certified under Good Manufacturing Practice (GMP) standards, featuring climate-controlled cleanrooms and automated packaging lines.

FSSAI Licensed Operations

Fully compliant with Food Safety and Standards Authority of India (FSSAI) Health Supplement regulations, adhering strictly to Indian RDA guidance.

Rigorous Batch Testing

Before release, each batch is tested by accredited laboratories for lead, cadmium, arsenic, mercury, yeast, mold, and active ingredient potency.

100% Transparent Labels

Zero undisclosed proprietary blends. Every bio-active ingredient, exact milligram dose, and percentage of daily requirement is declared clearly on the bottle.

Batch Verification

Certificate of Analysis (CoA) Lookup

Locate the 8-digit batch number stamped on the bottom of your bottle or carton box to verify accredited lab assay results.

Need an official certified copy for medical consultation? Email care@pharmlogicshealth.com with your bottle batch number.

Product Quality Inquiries & Pharmacovigilance

Pharmlogics takes consumer feedback seriously. If you have any questions regarding batch integrity, product seal, or storage stability, please contact our dedicated quality response team.

Quality Response Desk:care@pharmlogicshealth.com
Response Standard:Within 48 business hours

CLINICAL CONCIERGE

How can we help your journey?

Email Support

concierge@pharmlogics.com

Business Inquiry

registration #PL-24000447

Lab Location

Miami, Florida, USA

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*These statements have not been evaluated by the Food and Drug Administration.

COMMUNITY & PROTOCOLS

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