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WHO-GMP Compliant · ISO 9001:2015 Certified

Documented
pharmaceutical
manufacturing.

Established in 2022 in the pharmaceutical corridor of Himachal Pradesh, Rikencare Lifesciences manufactures syrups, capsules, drops and external preparations for brands that measure a supplier by documentation — not the quote at the bottom of the page.

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Approved Compositions
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Dosage Divisions
2022
Established
Rikencare monogram
WHO-GMP & ISO 9001:2015 Drug Lic. Form 25 & 28 Response Within 4 Hours IP / USP / BP Standards
Why Rikencare

Resilient. Robust. Refined.

Three words carry the brand — and every system serves them. We don't sell capacity. We sell peace of mind, backed by documented, repeatable proof.

R / 01

Resilient

Process discipline that holds under audit, scale and scrutiny — systems that don't bend when the order grows.

R / 02

Robust

GMP systems and batch consistency engineered to remove variance — the same medicine, every single run.

R / 03

Refined

A finish — and a paper trail — your brand is proud to ship to its own customers.

Capabilities

Four dosage divisions. One master brand.

A branded house — one logo, one palette, one voice — across every dosage form we manufacture under license.

Syrups & Suspensions

Cough, cold, analgesic, antacid, nutritional & enzyme liquids.

— SKUs

Capsules

SR / EC pellet capsules, PPI combinations & nutraceuticals.

— SKUs

Creams, Gels & Ointments

Antifungal, antibacterial, dermatological & analgesic topicals.

— SKUs

Drops & Solutions

Paediatric drops, oral solutions, mouthwash & antiseptics.

— SKUs
About Rikencare

A high-compliance partner — not a vendor.

Rikencare Lifesciences is a state-licensed third-party pharmaceutical manufacturer in Nalagarh, Himachal Pradesh — India's leading pharmaceutical corridor. We hold dual drug-manufacturing licenses under Form 25 and Form 28, covering 197 approved compositions.

  • State-licensed facility · Drug Mfg. License MNB/22/1197 & MB/22/1198
  • Liquid, capsule and external-preparation sections
  • Custom packaging — any bottle, label, cap and carton combination
  • Minimum order 3,000 units per SKU · for any query, we respond within 4 hours
Manufacturing License

Himachal Pradesh Health & Family Welfare Dept.

NO. HFW-H (DRUGS) 66/22

Form No. 25 · Granted 18/08/2022
MNB/22/1197
Form No. 28 · Granted 18/08/2022
MB/22/1198
Registered Facility

Vill. Messa Tibba, PO Manjholi, Tehsil Nalagarh, Distt. Solan, Himachal Pradesh

Product Portfolio

197 approved compositions.

A documented portfolio across syrups, suspensions, capsules, drops, solutions and external preparations — available for third-party, private-label and bulk manufacturing.

Trusted manufacturing for healthcare brands across India
FAQ

Frequently asked questions.

A partner your audit will trust.

Send us your product portfolio and receive a personalised quotation. For any query, we respond within 4 hours (Mon–Sat, 11 AM – 6 PM).

Our Products

197 approved compositions.

Browse the documented portfolio, configure packaging and build an enquiry. Minimum order 3,000 units per SKU. For any query, we respond within 4 hours.

Our Services

End-to-end manufacturing services.

From molecule to market — complete manufacturing, packaging and regulatory support, documented at every step.

Manufacturing Facility

A plant engineered for zero-defect output.

A GMP-compliant facility in Nalagarh, HP — three manufacturing sections built for precision, consistency and audit-readiness.

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Approved Compositions
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Manufacturing Sections
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Dosage Forms
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Documented Batches
Facility Tour

Every corner built to standard.

Liquid Section

Dedicated lines for syrups, suspensions, drops and solutions under controlled conditions.

Capsule Section

Precision filling of hard-gelatin capsules with EC/SR pellet technology and in-process controls.

External Preparations

Creams, gels and ointments manufactured in controlled, low-bioburden environments.

Quality Testing Labs

HPLC, UV, dissolution, microbiology and stability testing aligned to IP, BP & USP.

Packaging Area

Integrated primary and secondary packaging with premium, tamper-evident finishes.

Warehouse & Dispatch

Climate-controlled storage with serialised tracking and pan-India logistics.

Production Process

Raw material to finished goods.

STEP 01

Raw Material Inward

Vendor-approved inputs received & quarantined.

STEP 02

Inspection & QC

Identity, purity & specification testing.

STEP 03

Dispensing

Weighed & issued under controlled conditions.

STEP 04

Manufacturing

Produced to the master formula record.

STEP 05

In-Process Testing

Parameters verified at each critical stage.

STEP 06

Packaging

Primary & secondary to buyer specification.

STEP 07

Finished-Goods QC

Release testing against pharmacopoeial limits.

STEP 08

Dispatch

Documented release & logistics hand-off.

Quality Assurance

Quality is engineered — not inspected.

Every batch we manufacture passes documented in-process and finished-goods checks before it reaches your brand.

Quality Control

Documented in-process and finished-goods checks across every batch — signed and traceable.

Testing Standards

HPLC, UV, dissolution, microbiology and stability — aligned with IP, BP & USP.

Certifications

WHO-GMP compliance, ISO 9001:2015, dual drug-manufacturing licenses (Form 25 & 28) and state drug-authority approvals.

Safety Measures

Controlled environments, HVAC, cross-contamination prevention and operator-safety SOPs.

Research & Development

Formulation development, stability studies and delivery-system work under one roof.

Regulatory Compliance

Complete dossier preparation for CDSCO, FSSAI and export registration.

Certifications

Compliance you can verify.

About Rikencare Lifesciences

Manufacturing medicines your brand is proud to ship.

Driven by science, built on compliance — we make medicines that documentation, not adjectives, can vouch for.

Our Story

Established 2022. Licensed. Documented.

Established in 2022 in the pharmaceutical corridor of Himachal Pradesh, Rikencare Lifesciences manufactures capsules, syrups, drops and external preparations for brands that cannot afford a compromise. Our Nalagarh facility operates under dual drug-manufacturing licenses (Form 25 & 28), granted 18/08/2022, covering 197 approved compositions — WHO-GMP compliant, ISO 9001:2015 certified, documented and audit-ready.

We are built for the partner who measures a supplier by documentation, batch consistency and audit-readiness — not by the quote at the bottom of the page.

0
Approved Compositions
2022
Established
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Dosage Divisions
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Units · Min. Order
01

Our Mission

To manufacture high-quality, compliant medicines that empower healthcare brands and improve lives — with a documentation trail behind every batch.

02

Our Vision

To be the third-party manufacturing partner that R&D-driven, quality-led brands choose first — known for compliance and consistency.

03

Our Philosophy

Quality is non-negotiable. Compliance is the baseline. Partnership — documented, repeatable, audit-ready — is what we deliver.

Milestones

A path built on compliance.

2022

Established & Licensed

Rikencare Lifesciences founded at Nalagarh, HP, under dual drug-manufacturing licenses (Form 25 & 28) — MNB/22/1197 & MB/22/1198 — granted 18/08/2022.

2023

Sections Commissioned

Liquid, capsule and external-preparation sections brought online with GMP-compliant systems.

2024

Portfolio to 197

Approved-composition list expanded to 197 formulations across three manufacturing sections.

2026

Brand System v4.1

Unified the master brand — one logo, one palette, one voice — as a trust instrument for procurement leads.

Leadership

Led by industry veterans.

RS

Dr. Rakesh Sharma

Chairman & Managing Director

NK

Dr. Neha Kapoor

Chief Scientific Officer

AV

Ankit Verma

VP — Manufacturing

SI

Sara Iyer

Head of Quality Assurance

Careers

Build a career that impacts lives.

Join a team of pharmaceutical professionals who measure their work by documentation, consistency and patient impact.

Health Insurance

Coverage for you and your family.

Performance Bonus

Annual incentives & recognition.

Career Growth

Structured learning & development.

Quality-Led Culture

Collaborative & documentation-first.

Open Positions

Current openings.

Manufacturing

Production Manager

Nalagarh, HP
Full-time
Quality

QA Officer

Nalagarh, HP
Full-time
R&D · Formulation

R&D Scientist

Nalagarh, HP
Full-time
Regulatory

Regulatory Affairs Executive

Mumbai
Full-time
Get in Touch

Let's manufacture something great.

Tell us about your product — for any query, we respond within 4 hours (Mon–Sat, 11 AM – 6 PM).

Visit Us

Vill. Messa Tibba, PO Manjholi,
Tehsil Nalagarh, Distt. Solan,
Himachal Pradesh — 174101

Call Us

+91 98160 00000

Email Us

info@rikencare.com

Working Hours

Mon – Sat
11:00 AM – 6:00 PM IST

Enquiry

Request a manufacturing quote.

For any query, we respond within 4 hours (Mon–Sat, 11 AM – 6 PM IST).

Enquiry received.

Thank you — your enquiry has been submitted successfully. For any query, we respond within 4 hours (Mon–Sat, 11 AM – 6 PM IST).

Rikencare Lifesciences — Unit 1Vill. Messa Tibba, PO Manjholi, Tehsil Nalagarh,
Distt. Solan, Himachal Pradesh — 174101
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