
Reliable Guidance	*The Experts in Clinical Trial Materials Management™*

SOPs

	Templates to meet all regulatory requirements and guidelines (cGMP, GCP, GLP, DEA, and ICH)
	Customized to meet your company's needs
	Includes:
		Purpose
		Scope
		Procedure
		Responsibilities
		References & related documents
		Checklists (if applicable)
	Review and authoring of existing SOP's
	QA approval
	Annual review
	21 CFR Part 11 Compliance
Full Sample SOP Below (Click to Open Document)

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