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公司新闻:
- Customs clarifies requirements for the duty-free importation of . . .
New Zealand Customs Service (NZ Customs) has reviewed the treatment of drugs and other material imported solely for the purposes of clinical trials Customs had previously allowed the entry of these goods as samples under Regulation 65 of the Customs and Excise Regulations 1996 (C E Regs 1996)
- Steps to importing research samples (excluding animal samples)
Understanding and meeting your biosecurity requirements when importing research samples and materials can be difficult We've created a step-by-step process to help you On this page, we outline the steps you need to follow to bring in research samples
- Regulations | nzacres. org. nz
Transporting Clinical Trial Materials New Zealand is well connected to important international centres via global transportation networks Importing Materials All imports into New Zealand are subject to Ministry for Primary Industries (MPI) and New Zealand Customs Import regulations
- New Zealand - Clinical Trial Regulatory Process - Credevo Articles
Materials used in Clinical trials All imports into New Zealand are subject to the Ministry of Agriculture Forestry (MAF) and New Zealand Customs Import regulations A commercial invoice is required to accompany all goods Clinical trial statistics in New Zealand
- Guideline on the Regulation of Therapeutic Products in New Zealand
Under section 30 of the Medicines Act, approval from the Director-General of Health is required before a clinical trial using a new medicine may commence in New Zealand The approval process for clinical trials is administered by Medsafe
- Clinical Trials in NZ | HealthTech Activator - Callaghan Innovation
All imports into New Zealand are subject to the Ministry for Primary Industries (MPI) and New Zealand Customs Import regulations Detailed information about New Zealand’s importing requirements can be found on the MPI website You can read more about materials shipping on the NZ Association of Clinical Research (NZACRes) website
- Managing Importation Requirements for Your Products
Identify ways to navigate the complex regulations involved in the import and export of clinical trial supplies and ensure compliance; Articulate the accountability and responsibilities of the owner, the importer exporter of record, and the customs broker; Describe a record-keeping practice that would ensure appropriate
- Clinical Trial Logistics - Pharma Logistics NZ
Validated packaging and applicable temperature monitoring technology to protect materials at all stages of transit; Our regulatory and trade compliance experts undertake all import and export processes; Specialist in house project managers who understand and handle all aspects of the clinical trial logistics process, including gateway services
- Step By Step Guide To Importing Goods Into New Zealand (2025 Updated)
Importing goods into New Zealand may appear complex, but following these 6 detailed steps can considerably simplify the process in 2025 The key is to approach each stage methodically, ensuring you fully understand your legal and financial obligations along the way
- The Regulation of Clinical Trials in New Zealand
NZCR undertakes clinical trials in NZ under strict regulatory controls to ensure the trial is conducted safely, ethically, with scientific rigour Learn more about the regulation of clinical trials in NZ
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