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PRESS RELEASE Nagoya Protocol sees new ratification and issuance of second internationally recognized certificate of compliance Montreal, 29 March 2016 Following the ratification by Senegal, the total
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01
Read and understand the Nagoya Protocol thoroughly.
02
Identify if your activities fall under the scope of the Nagoya Protocol.
03
Obtain the necessary permits and permissions from the relevant authorities.
04
Collect all the required information about the genetic resources you intend to access or use.
05
Negotiate mutually agreed terms (MAT) with the providers of genetic resources.
06
Ensure compliance with ABS obligations and benefit-sharing arrangements.
07
Keep records of all transactions and access to genetic resources.
08
Regularly review and update your compliance with the Nagoya Protocol.
09
Report any relevant information to the appropriate national focal points.
10
Seek legal advice or guidance if needed.

Who needs nagoya protocol sees new?

01
Researchers and scientists conducting studies that involve access to genetic resources.
02
Pharmaceutical and biotechnology companies developing products derived from genetic resources.
03
Traditional knowledge holders and indigenous communities whose resources are being accessed.
04
Government agencies responsible for regulating access and benefit-sharing of genetic resources.
05
Biodiversity conservation organizations and initiatives.
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The Nagoya Protocol sees new regulations for access to genetic resources and the fair and equitable sharing of benefits arising from their utilization.
Any individual or organization that wishes to access genetic resources for research or commercial purposes.
To fill out the Nagoya Protocol, one must provide detailed information on the genetic resources being accessed, the intended use, and the benefit-sharing plan.
The purpose of the Nagoya Protocol is to ensure the conservation and sustainable use of genetic resources and to promote fair and equitable sharing of benefits.
Information such as the source of genetic resources, details of access permits, benefit-sharing agreements, and any relevant research or commercial activities.
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