
Simplify Your Pharmaceutical Ingredient Verification Process in Hong Kong
If you have any questions about our services, please leave us a message. We are delighted to assist you.
Streamline and Expedite
Your Pharmaceutical Ingredient Verification Process with
Premia TNC
Streamline and Expedite Your Pharmaceutical
Ingredient Verification Process with Premia TNC
Working around the regulations for pharmaceutical products in Hong Kong can turn into a daunting task, particularly when it comes to ingredient verification. The Pharmaceutical Ingredients Check is a critical step in the licensing process, ensuring that all components used in your products comply with established safety standards and are authorized for market use.
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With Premia TNC’s expertise, your business can benefit from

Accelerated Time-to-Market
We streamline the ingredient verification process to help you reduce regulatory delays and bring your products to market faster.

Regulatory Compliance Assurance
Our team ensures that all pharmaceutical ingredients meet the health and safety requirements mandated by Hong Kong’s authorities.

Risk Mitigation
Avoid fines, product recalls, and approval setbacks through comprehensive checks and expert handling of regulatory documentation.

Specialized Expertise
With in-depth knowledge of pharmaceutical regulations, Premia TNC provides guidance and support throughout the verification process.
By partnering with Premia TNC, you can work around regulatory challenges with a breeze, maintain utmost compliance, and focus on expanding your presence in the pharmaceutical market.
Fast-track the Registration Screening Process with
Three Simple Steps:
Step 1
Information
Begin by providing the following details to initiate the registration process:
Provide the product indication and the active ingredient for checking.
This information allows us to evaluate compliance with Hong Kong’s food and drug safety standards.
Step 2
Review
Upon submission, our team will:
3 working days reporting by email after the service fee and the required documents are received.
Step 3
Product Registration
After confirming the ingredients in your product, you may proceed to the next steps, which involve registering a new pharmaceutical product and applying for registration as a Wholesale Dealer.
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Primary Factors for Registration
for Pharmaceutical Ingredient Check Handling

Requirements to Register
Any person or entity engaged in the handling of pharmaceutical ingredients for the purposes of trading, manufacturing, packaging, or distribution must obtain registration under the PR Class. This includes activities related to the preparation of pharmaceutical products that involve the use of active ingredients. The applicant must ensure that the premises and operations conform to Good Manufacturing Practice (GMP) standards and are suitable for the intended purpose. Separate registrations are required for different classes or business locations.

Qualifications and Credentials
Applicants must possess a valid business registration and demonstrate that they employ appropriately qualified personnel, such as pharmacists or technical staff with relevant pharmaceutical training. They must also maintain adequate documentation systems and quality assurance protocols to ensure safety and regulatory compliance. The responsible person-in-charge should have sufficient experience and understanding of GMP and handling of pharmaceutical substances. Additionally, facilities must be equipped to meet environmental, safety, and hygiene requirements as prescribed by the Pharmacy and Poisons Board.
Why People Trust Us
We extend special thanks to our partners.
We have a long history of working with various sizes of corporation of renowned brands.







































































Our Clients Rely On Our Expertise
We have worked with 6,000+ clients and Partners 90% of our clients recommend us
Here’s what our clients have to say:
Arnav Singh.
Yunxiu Wang.
Julia Kim.
Anushka Agarwal.
Monish Patel.
Pang Jiawei.
Frequently Asked Questions
1. What is the typical timeframe for a Pharmaceutical Ingredients Check?
2. What documents are required for the Pharmaceutical Ingredients Check?
3. What is the cost of the Pharmaceutical Ingredients Check Handling service?
The service fee is determined based on the complexity and specifications of your product. For an accurate quote, please contact us directly.
4. Does Premia TNC offer other regulatory services besides the Pharmaceutical Ingredients Check?
5. How can I initiate the Pharmaceutical Ingredients Check Handling service?
Still carrying concerns?
Reach out today and speak with our expert consultants.
