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Regulatory Support Services by TRC

The services listed below represent TRC’s commonly requested regulatory support offerings, including subscription plans and  product notifications services.

For complex projects or customised scopes, clients typically engage with us directly. The listings here are intended as a reference to help you understand available service types and indicative pricing.

How TRC’s Regulatory Support Services Are Typically Engaged

TRC supports pharmaceutical, medical device, cosmetic, health supplement and TCM companies across different stages of the product lifecycle.

Depending on the product type, market, and regulatory pathway, clients may engage TRC for pre-licensing activities such as gap analysis and regulatory intelligence, or for post-licensing support including licence maintenance, variations, change notifications, renewals and post-market regulatory activities, as applicable to the selected service or agreed scope of work.

FAQs About TRC 's Regulatory Support Services

The listed services represent common regulatory support offerings and engagement formats. Actual regulatory scope depends on the product type, regulatory pathway and applicable authority requirements, and is confirmed with clients as part of the engagement discussion.

Regulatory Affairs Subscription Plans are typically engaged by companies with lean regulatory teams or without an in-house regulatory presence in Singapore or the region. Under these arrangements, TRC acts as an external regulatory consultant supporting ongoing regulatory activities across products, markets or lifecycle stages, as agreed within the scope of work. The suitability and structure of a subscription plan are usually discussed with clients based on workload, product portfolio and regulatory complexity.

TRC supports notification-based regulatory pathways for products such as cosmetics, health supplements, TCM and other borderline products. Support may include product classification assessment, review of formulation and claims, and preparation or review of notification documentation, depending on the applicable regulatory requirements. Clients are encouraged to contact TRC to discuss their product details and target market so that the appropriate notification pathway can be confirmed.

Hand picking pharmaceutical product for regulatory consulting in pharma
If you have any specific regulatory questions pertaining to entering the Singapore market or require assistance with pharma regulatory services and medical product registration, feel free to reach out. Your success in the pharmaceutical industry starts with us!

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