Acts and Guidelines
Acts and Guidelines are legal and regulatory documents that provide guidance and rules for various activities, including those related to healthcare, research, and clinical trials.
Acts and guidelines provide a clear and consistent framework for regulating and conducting clinical trial activities. They ensure that activities are carried out in a safe, ethical, and effective manner, by holding individuals and organizations accountable to a set standard. Additionally, acts and guidelines help promote international harmonization and consistency in regulatory requirements and facilitate the development and approval of new products and therapies.
Here we have listed all the acts and guidelines you may require from start to finish.
Acts and Guidelines
Declaration of Helsinki – The World Medical Association
Health Services Act 1988 – Victoria
Health Records Act 2001 – Victoria
Statutory Guidelines on Research – Health Records Act 2001 (Vic)
Medical Research Future Fund Act 2015 – Victoria
Mental Health Act 2014 – Victoria
Drugs, Poisons and Controlled Substances Regulations 2017 – Victoria
Public Health and Wellbeing Act 2008 – Victoria
Privacy and Data Protection Act 2014 – Victoria
Freedom of Information Act 1982 – Victoria
Charter of Human Rights and Responsibilities Act 2006 – Victoria
Medical Treatment Planning and Decisions Act 2016 – Victoria
Australian Institute of Aboriginal and Torres Strait Islander Studies Act 1989
Guidelines under Section 95 of the Privacy Act 1988 | NHMRC – Conduct of Medical Research
Guidelines approved under Section 95A of the Privacy Act 1988 | NHMRC – Conduct of Medical Research