Market Access.
Regulatory Excellence.
Business Growth.

Helping businesses navigate approvals, certifications, licensing, and compliance requirements across healthcare, food, cosmetics, electronics, manufacturing, environmental, and consumer product sectors.

With expertise spanning CDSCO, Medical Devices, BIS, Legal Metrology, FSSAI, ISO Certifications, EPR Compliance, and Regulatory Advisory, we help organizations move from compliance uncertainty to commercial certainty.

70 +
Business Supported
400 +
Regulatory Projects Assisted

Multi Industry Expertise

End-to-End Compliance Ownership

Join over +15,000 happy clients!

Beyond Compliance
Built For Business Growth.

Most consulting firms focus on paperwork.

We focus on business outcomes.

LexAccord Global is a multidisciplinary consulting firm helping businesses overcome regulatory barriers that delay product launches, market expansion, manufacturing operations, imports, exports, and government approvals.

Our team combines regulatory specialists, legal advisors, technical consultants, quality professionals, and market access experts to create structured compliance pathways that reduce risk and accelerate business growth.

Whether you are a startup introducing your first product, a manufacturer expanding production capabilities, or a multinational company entering India, we provide strategic guidance throughout the regulatory lifecycle.
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Since
Our Services

We are here to solve your problem and deliver your needs

Regulatory Compliance

Navigate complex regulatory requirements with end-to-end support for licensing, approvals, and compliance management across regulated industries.

Product Certifications

Achieve product compliance and market readiness with expert certification solutions that help your products meet national and international regulatory standards.

Food & Consumer Compliance

Ensure your food and consumer products comply with statutory regulations through licensing, registrations, labelling, and market access support.

Business & Legal
Compliance

Protect your business with strategic legal advisory, regulatory due diligence, contract support, and compliance solutions designed to reduce risk and strengthen governance.

Environmental
Compliance

Meet environmental obligations through comprehensive EPR and compliance solutions that support sustainable business operations and regulatory adherence.

Laboratory & Technical Consulting

Build and optimize compliant laboratories with expert guidance on infrastructure, equipment selection, installation, calibration, validation, and maintenance.

Training & Skill Development

Empower your workforce with industry-focused training programs that strengthen regulatory knowledge, operational excellence, and compliance culture.

Market Access

Accelerate your expansion into regulated markets with strategic market access, regulatory planning, and local representation services for domestic and international businesses.

Corporate Advisory

Drive sustainable business growth through expert advisory on business formation, corporate restructuring, governance, licensing, and ongoing statutory compliance.

Our Regulatory Success Framework

A Structured Approach to Faster Market Access

Frequently Asked Questions

Answers to Common Regulatory Questions.

What is CDSCO Registration ?
CDSCO (Central Drugs Standard Control Organization) registration is the regulatory approval required to import, manufacture, or market drugs, cosmetics, and medical devices in India. We manage classification, documentation, submission, and liaison end-to-end.
 
Any importer, manufacturer, or distributor of notified medical devices and IVDs requires registration under the Medical Devices Rules. Class A, B, C, and D devices each follow distinct pathways under MD-14/MD-15 and related forms.
 
Timelines vary by scheme – typically 60 to 120 working days for ISI, and 20 to 60 working days for CRS – depending on testing, factory inspection, and queries. We sequence steps to minimize friction.
Healthcare, pharmaceuticals, medical devices, food, cosmetics, electronics, electrical, mechanical, automotive, manufacturing, importers/exporters, hospitals, consumer goods, government suppliers, e-commerce brands, MSMEs, and large enterprises.
 
Yes. From regulatory assessment and documentation to submission, government liaison, approval, and post-approval compliance, we own the full lifecycle with dedicated project managers.
 
Absolutely. We routinely secure import licenses (MD-15, drug imports, cosmetic registrations), manufacturing licenses, factory approvals, and related state-level permissions.
Yes. We support overseas manufacturers and global brands with India entry strategy, authorized Indian representation, regulatory registrations, and ongoing compliance management.
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20Jul

Government Proposes Major Reforms to…

The Ministry of Health and Family Welfare has proposed significant…

Medical Devices Rules 2017 Amendment: Government Proposes Faster Manufacturing Licence Approvals
05Jul

Medical Devices Rules 2017 Amendment:…

The Ministry of Health and Family Welfare has proposed amendments…

Drug Registry Launched Under Ayushman Bharat Digital Mission: A Major Step Towards Standardized Digital Healthcare
03Jul

Drug Registry Launched Under Ayushman…

The Government of India has launched the Drug Registry under…