ASTM F2103-01(2007)

ISO 13408-1: 1998:

Aseptic Processing of Health Care Products--Part 1: General Requirements

Ph. Eur.

Monograph Chitosan Chloride, Nov. 2000 Available from EDQM, Publications and Services European Pharmacopoeia, BP 907 226, avenue de Colmar, F-67029 Strasbourg Cedex 1, France.

F1906-98

Standard Practice for Evaluation of Immune Responses In Biocompatibility Testing Using ELISA Tests, Lymphocyte, Proliferation, and Cell Migration

F895-11(2016)

Standard Test Method for Agar Diffusion Cell Culture Screening for Cytotoxicity

F813-20

Standard Practice for Direct Contact Cell Culture Evaluation of Materials for Medical Devices

F763-22

Standard Practice for Short-Term Intramuscular Screening of Implantable Medical Device Materials

F756-17

Standard Practice for Assessment of Hemolytic Properties of Materials

F749-20

Standard Practice for Evaluating Material Extracts by Intracutaneous Injection in the Rabbit

F748-16

Standard Practice for Selecting Generic Biological Test Methods for Materials and Devices

F619-20

Standard Practice for Extraction of Materials Used in Medical Devices

D2196-20

Standard Test Methods for Rheological Properties of Non-Newtonian Materials by Rotational Viscometer

F1905-98

Standard Practice for Selecting Tests for Determining the Propensity of Materials to Cause Immunotoxicity

F1251-89(1995)

Standard Terminology Relating to Polymeric Biomaterials in Medical and Surgical Devices

F981-23

Standard Practice for Assessment of Muscle and Bone Tissue Responses to Long-Term Implantable Materials Used in Medical Devices

F1904-23

Standard Guide for Testing the Biological Responses to Medical Device Particulate Debris and Degradation Products in vivo

F1903-18

Standard Practice for Testing for Cellular Responses to Particles in vitro

F1439-03(2018)

Standard Guide for Performance of Lifetime Bioassay for the Tumorigenic Potential of Implant Materials