Artixio

Product Registration Services in Singapore for Life Sciences

Expert support for product registration in Singapore across all life sciences sectors: From compliance to final approval, our Singapore-based consultants guide your product through HSA registration.

Trusted Services for Product Registration in Singapore

At Artixio, we specialize in managing the entire product registration process in Singapore, making sure your product meets all necessary regulatory requirements for approval. Our team handles every step, from initial registration to post-market support, ensuring a smooth transition to market release.

Singapore Product Approval with Expert Consultants

We begin by understanding the unique needs of your product across various sectors like pharmaceuticals, medical devices, cosmetics, nutrition, biologics, and veterinary products.
Artixio guides you through the process of documentation preparation, submission, and communication with the local regulatory authorities.
We streamline approvals, working closely with the Health Sciences Authority (HSA) to meet all requirements for your product’s market entry.

Product Registration Process in Singapore

We manage the entire lifecycle of product registration in Singapore

We determine the product classification to identify the applicable regulations.
Prepare all necessary documentation, including safety data, clinical trials, and labeling to meet HSA requirements.
Submit the complete documentation to the Health Sciences Authority (HSA) for review.
Then HSA reviews the submission, and we manage follow-up requests to ensure a smooth process.
Once approved, we assist with market entry and post-market surveillance.

Why Partner with Artixio for Product Registration in Singapore

FAQs

What is the first step in the product registration process in Singapore?
The first step is determining your product classification, which helps identify the applicable regulations for registration.
Yes, if you are a foreign company, a local representative or authorized agent is typically required to liaise with the Health Sciences Authority (HSA).
Artixio supports ongoing compliance and product monitoring through post-market surveillance services, ensuring your product remains in compliance after approval.
The HSA is the regulatory body responsible for reviewing product submissions, ensuring they meet the required safety and quality standards before approval.

Still Have Questions ?

Get expert answers tailored to your needs.

Specialized Registration Services Across Multiple Industries

Pharmaceuticals

MedTech

Cosmetics

Nutrition

Biologics

Veterinary

Expert Regulatory Services To Streamline Compliance

Regulatory Intelligence & Strategy
Medical & Technical Writing
Publishing & Submission
Product Registration
Investigation New Drug Application (IND)
New Drug Application (NDA)
Post Approval Lifecycle Maintenance
Artwork and Label Review
Ad Promo Review

Regulatory Affairs Across Multiple Countries

India

Singapore

Mexico

Brazil

Vietnam

Malaysia

Argentina

Colombia

Taiwan

China

European

Thailand

Indonesia

Philippines

USA

Japan

Qatar

South Korea

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