Simplify Your Pharmaceutical Ingredient Verification Process in Hong Kong

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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.


A Trustworthy firm, serving 6,000+ clients in corporate matters

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

Submit Product
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

Screening and
Review

Upon submission, our team will:
3 working days reporting by email after the service fee and the required documents are received.

Step 3

Certification and
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.

Ensure your pharmaceutical product meets Hong Kong’s regulatory requirements and start your registration process today.

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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:

Frequently Asked Questions

1. What is the typical timeframe for a Pharmaceutical Ingredients Check?
Once the service fee and required documents are received, you will receive the report within two working days. This efficient turnaround helps you stay on track with product registration timelines.
To proceed with the check, you need to provide the product indication, which explains the intended use of the product, along with detailed information about the active ingredients, including their chemical composition and supplier information.

The service fee is determined based on the complexity and specifications of your product. For an accurate quote, please contact us directly.

Yes, our Trading Team offers a comprehensive range of regulatory services, including product registration, import and export licensing, and customs compliance, to support your business needs.
To get started, simply reach out to us with your product details and the necessary documents. We’ll guide you through the next steps for a smooth and efficient process.