From Concept to Commissioning•35+ Years in Greenfield API & Intermediate Facilities•Founder & Director: R.K. Mishra
+91 85117 20749|rkmishra@jhpharmacon.com|Ahmedabad, Gujarat, India
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J&H API Pharma ConsultantsFrom Concept to Commissioning

J&H API Pharma Consultants Specialises in Design & Detail Engineering for Greenfield API Pharma & Intermediate Projects. Complete end-to-end execution under one disciplined roof.

From Concept to Commissioning.
35+ Years · 100+ Greenfield Plants · 500+ QbD Checkpoints
+91 85117 20749rkmishra@jhpharmacon.com
1115, 11th Floor, Fortune Business Hub, Sola, Hebatpur, Near Shell Petrol Pump, Science City Road, Sola, Ahmedabad-380060, Gujarat
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Key Disciplines
  • Master Site Planning
  • API Plant & P&ID Translation
  • ISO Class 8 Cleanroom & HVAC
  • RCC Slabs & 150 Pre-Cast Cutouts
  • Utility Line Diagrams & Isometrics
  • 415V/11kV PCC & Flameproof SLD
  • On-Site Slab Clearances & FAT
Project Consultant
R.K. Mishra
Director — Projects
J&H API Pharma Consultants, India
rkmishra@jhpharmacon.com+91 85117 20749
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Engineering API Pharma Facilities for Quality, Compliance & Efficiency. · Design & Developed by Sharvaya Infotech.
J&H API Projects
INDUSTRIES & APPLICATIONS

100+ PROJECTS. THREE DECADES OF EXPERIENCE.

With hands-on technical experience spanning over 35 years and 100+ greenfield projects, J&H API Pharma Consultants has designed state-of-the-art facilities across all major API sectors.

01
COMPLEX API SYNTHESIS01

Chemical Synthesis

Multi-stage multi-reactor chemical synthesis facilities engineered for halogenation, nitration, catalytic hydrogenation, and high-temperature cyclization with complete solvent recovery systems.

02
POTENT STEROID BLOCK02

Steroids

High-containment processing suites designed to handle active corticosteroid and steroid chemistry, preventing occupational exposure and cross-contamination.

03
HIGHLY POTENT API (HPAPI)03

Hormones

Dedicated segregated hormone production blocks engineered with specialized air handling units and HEPA filtration.

04
NUTRACEUTICAL & BULK VITAMINS04

Vitamins

Large-capacity bulk API vitamin manufacturing complexes featuring continuous crystallizers, rotary vacuum dryers, and automated high-throughput processing.

05
CYTOTOXIC API BLOCK05

Oncology

High-potency cytotoxic API facilities incorporating OEB 4 / OEB 5 containment barriers, isolators, closed powder transfer, and specialized waste treatment.

06
ADVANCED API PHARMA INTERMEDIATES06

API Intermediates

High-capacity greenfield manufacturing plants for critical starting materials and advanced intermediates, designed for maximum batch cycle efficiency.

REGULATORY COMPLIANCE

ENGINEERED AROUND REGULATORY EXPECTATIONS.

Our design and detail engineering methodologies are developed around major national and international regulatory frameworks, ensuring plants are auditable and compliant with multinational customer standards.

cGMP

Current Good Manufacturing Practice

Cleanroom segregation, airlocks, unidirectional material movement, and contamination containment.

WHO TRS

World Health Organization Guidelines

Technical Report Series for active API pharmaceutical ingredient production facilities and sterile processing.

USFDA 21 CFR

Title 21 CFR Part 210 / 211

Auditable facility engineering, cleanroom classification, computerized BMS monitoring, and qualification.

EU GMP

European Guidelines (Annex 1)

Differential pressure cascades, viable/non-viable particulate control, and cleanroom air handling standards.

GEP

Good Engineering Practice

Cost-effective, robust engineering lifecycle from design basis to installation, testing, and handover.

ISO 14644

Cleanrooms & Associated Controlled Environments

ISO Class 8 / Grade D area validation, air change rates (ACPH), and ISO 14644-3 on-site testing procedures.

IS CODES

Bureau of Indian Standards (BIS)

IS 456-2000 for concrete, IS 800-2007 for steel, IS 3043 for electrical earthing, and NBC fire safety norms.

NOTE: Referenced frameworks reflect J&H's engineering design standards to meet client expectations and audits.
WHO / USFDA AUDIT COMPLIANT DESIGNS