At Jinglong Biotechnology, we often receive customer inquiries:

"Do you have export qualifications?"

"What standards do your production workshops meet?"

"How do you ensure the quality stability of all batch of products?"

Q1: Can Jinglong Biotechnology's products be exported to the United States?

Yes. We have completed U.S. FDA registration.

What does this mean?

FDA registration is not an optional certification, but a mandatory legal requirement for products exported to the United States. Completing FDA registration means:

• Our production facilities and enterprise information have been filed on the official U.S. FDA website;

• Our quality management system is supervised by U.S. regulations;

• Our products have the legal qualification to enter the U.S. market.

Benefits for you:

If you are looking for a pet oral dispersible film supplier that can export to the North American market, Jinglong Biotechnology is a compliant choice. FDA registration information supports offline verification by customers  to provide a reliable foundation for cooperation.

Q2: How do you ensure food safety during production?

We have established the ISO 22000 food safety management system, with full control from raw materials to finished products.

What does this mean?

ISO 22000 is a globally recognized food safety management standard. Obtaining this certification proves that we:

• Full-process control: All links from raw material procurement, production and processing to finished product delivery are under system control;

• Risk identifiable: A systematic hazard identification and risk assessment mechanism is established to know where risks are and how to control them;

• Continuous improvement: Regular internal audits and management reviews are conducted to continuously optimize the management system.

Benefits for you:

Choosing a supplier certified by ISO 22000 means the products you receive benefit from a systematic, predictable, and consistently stable quality assurance process.

Q3: How do you prevent food safety issues?

We adopt the HACCP system to eliminate risks during the production process.

What does this mean?

The  key difference between HACCP and traditional quality inspection is: it does not check products after they are made, but controls risks during production.

Hazard Analysis: We analyze each stage of the production process to identify potential biological, chemical and physical hazards;

• Critical Control Points: Set monitoring points at key links where hazards may occur;

• Prevention first: Immediately correct deviations from standards to prevent problems from flowing to the next process.

Benefits for you:

The HACCP system is equivalent to an “early warning system” for the production process. Each batch of oral dispersible film you receive is produced under the monitoring of dozens of critical control points,  ensuring product safety.

Q4: What is the production workshop environment like? What standards does it meet?

We strictly follow cGMP (Current Good Manufacturing Practices), have passed the audit of the international certification body BV, and the workshop meets the 100,000-class clean standard.

What does this mean?

cGMP is not a certificate, but a standard that must be implemented in daily operations. It runs through:

• Workshop environment: 100,000-class clean workshop with filtered air and constant temperature and humidity;

• Personnel management: Strict hygiene standards require changing clothes and disinfection before entering the workshop;

• Equipment cleaning: Equipment is cleaned according to specified procedures before and after every batch of production;

• Document records: All operations are recorded, and all steps are traceable.

Special note:

Our workshop is equipped with observation windows to facilitate supervision of the production process by customers and the public. We believe: transparent production is reassuring production.

Benefits for you:

cGMP is the foundation for the effective operation of HACCP and ISO 22000. Without standardized daily operations, management systems may not be effectively implemented. We adhere to cGMP standards in daily production to ensure consistent quality.

Q5: What do so many qualifications really mean for customers?

We summarize the value of the four major qualifications in a table:

The integration of four certifications means:

• If you care about export qualifications — we have FDA registration;

• If you care about management systems — we have ISO 22000;

• If you care about risk prevention — we have HACCP;

• If you care about the production site — we have cGMP and a transparent workshop.

[Qualification Verification]

We welcome customers to verify our qualifications.

• FDA Registration: Supports offline verification of registration information by customers;

• ISO 22000 Certificate: Scanned copy of the certificate is available;

• HACCP Certificate: Scanned copy of the certificate is available;

• cGMP Implementation: Welcome to make an appointment to visit the workshop and witness the production environment in person.