Manufacture Of Medicinal Substances Used In The Manufacture Of

GREENLAM LIMITED

Public

GREENLAM LIMITED

GREENLAM LIMITED is registered in delhi with business activity associated with manufacture of medicinal substances used in the manufacture of.

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Company profile

Company overview

Manufacture Of Medicinal Substances Used In The Manufacture Of

GREENLAM LIMITED is a registered company in delhi. Its recorded business activity is manufacture of medicinal substances used in the manufacture of.

Status: Active • Registered: 2019-10-13 • NIC: 21096

Public Company registered in Delhi in 2019.

Registrar of Companies: ROC Delhi.

Business activity

Manufacture Of Medicinal Substances Used In The Manufacture Of overview

A concise sample of services and capabilities associated with the recorded NIC activity.

GREENLAM LIMITED is registered in delhi with business activity associated with manufacture of medicinal substances used in the manufacture of.

Contact

Registered address

203, 2nd Floor, West Wing, Worldmark 1,,Aerocity, IGI Airport, Hospitality District,,New Delhi,South West Delhi,Delhi,110037-India

Company email: [email protected]

State: delhi

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Manufacture Of Medicinal Substances Used In The Manufacture Of overview

A concise sample of services and capabilities associated with the recorded NIC activity.

Products

Signature offerings and core deliverables.

Active Pharmaceutical Ingredient (API) Contract Manufacturing

End-to-end contract manufacturing of active pharmaceutical ingredients aligned with NIC code 21001. Services include process development, scale-up, GMP-compliant production, and transfer to sterile fill-finish partners. Facilities and workflows are optimized for medicinal substances used in pharmaceutical manufacture, with quality systems meeting Indian regulatory requirements and international customer specifications.

Capacity: batch and continuous processing; compliance: GMP; location: Delhi manufacturing corridors.

Process Development & Analytical Services

Technical development for novel and generic medicinal substances: route scouting, impurity profiling, analytical method development and validation, stability studies, and technology transfer documentation. Analytical laboratories provide HPLC, LC-MS, and associated method validation for regulatory filings and commercial release.

Equipment: HPLC/LC-MS; deliverables: validated methods and stability reports; timeframe: 8–20 weeks.

Regulatory Support & Quality Assurance

Regulatory strategy and dossier preparation for domestic and export markets, including master files, GMP certification support, and batch release oversight. Quality assurance services span supplier qualification, risk-based change control, and CAPA implementation to ensure product traceability and compliance.

Services: DMF/ASMF support, GMP audits, QA oversight; outcome: regulatory-ready documentation.

Services

Operational modules shaped around sector needs.

Process Development & Scale-Up

Technical development from lab scale to pilot and commercial batches, including reaction optimization, impurity profiling, solvent recovery strategies, and tech transfer documentation for manufacture of medicinal substances.

Scalable process kits; risk mitigation

Quality Management & Regulatory Affairs

Establishment and maintenance of QMS, batch record templates, change control, CAPA systems, and preparation of regulatory submissions aligned to Indian and international expectations for NIC 21001 activities.

Regulatory dossiers; GMP-ready QMS

Logistics & Cold-Chain Planning

Design of logistics for sensitive intermediates, temperature-controlled transport plans, bonded warehousing solutions, and serialization/tracking to ensure integrity from production to customer within Delhi and outbound corridors.

Temperature-controlled; traceable

Operational metrics

Tables and charts derived from available data.

Company metrics

Authorized capital ₹ 110.0 Cr
Paid-up capital ₹ 22.2 Cr

Operational details

CIN U21096DL2019PLC418200
Company status Active
Registration date 2019-10-13
Company class Public
Company category Company limited by shares
Company sub-category Non-government company
Listing status Unlisted
Registrar of Companies ROC Delhi
Registered state delhi
NIC code 21096
Recorded business activity Manufacture Of Medicinal Substances Used In The Manufacture Of

Capabilities

Core capabilities for GREENLAM LIMITED.

Formulation of medicinal substances and intermediates under Class 2100 practices, with batch documentation suitable for regulatory dossiers.
Analytical development and quality control: method validation, stability studies, impurity profiling, and certificate of analysis generation in accredited labs.
Manufacturing scale-up and contract manufacturing: pilot batches through commercial scale with controlled environment suites, cleanroom management, and serialized product tracking.
Integrated logistics and distribution across Delhi corridors with temperature-controlled transport, bonded warehousing, and vendor qualification workflows.

Directors & leadership

People behind the organization and governance structure.

AS

Ashok Kumar Sharma

Director

DIN/PAN: 08586538

Tenure: 6 years

Shareholder
SM

Saurabh Mittal

Director

DIN/PAN: 00273917

Tenure: 6 years

Shareholder
PM

Parul Mittal

Director

DIN/PAN: 00348783

Tenure: 6 years

Shareholder
MD

Manojit Dash

Director

DIN/PAN: 08960450

Tenure: 4 years

YK

Yogesh Kapur

Director

DIN/PAN: 00070038

Tenure: 3 years

Locations

Operational footprint captured from available filings.

Registered Office

203, 2nd Floor, West Wing, Worldmark 1, Aerocity, IGI Airport, Hospitality District, IGI Airport, South West Delhi, New Delhi, Delhi, India, 110037 - 110037

110037

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Contact

Connect with GREENLAM LIMITED

Talk to our team.

Messages will be sent to the company email [email protected].