[87A. Registration certificate to sell, stock, exhibit or offer for sale or distribut ...

e) a description of the accessories, other medical device and other product that are ...

(iv) ISO-10993, Biological Evaluation of Medical Devices, should be followed for cond ...

7. Quality Assurance: Description of the quality assurance system and of the activiti ...

85. Conditions of registration A registration granted under sub-rule (3) of rule 83 i ...

1.4 If a manufacturer engages in only some operations subject to the requirements of ...

ACPL's expertise in navigating the regulatory landscape of medical research contribut ...

2.0 Device description and product specification, including variants and accessories ...