Simplimedica Ltd

Regulatory authorities are now more watchful of Medical Device industry than ever before resulting in warning letters, 483's. or even observations which can effect your companies reputation and having licences revoked. Simplimedica Ltd. is experienced in ensuring you achieve satisfactory audits, whether you are submitting a 510K application or maintaining your validation system. Simplimedica Validation consultants are experienced in assisting start up scale businesses as well as multinational businesses. You can hire our services, whether it is initial risk assessment through to advice on validations, or performing qualification at Installation, Operation or Performance, or perhaps full project management from the initial stages of equipment purchase through to commissioning and handover to production. You may want us to give you training or provide you with templates so that you may perform your own validations, just pay and download. Either way Simplimedica Validations can help you on your regulatory journey. Contact us for a confidential conversation or a no obligation quote: