Regulatory, QA and PV activities

Tzamal Biopharma has its own in-house regulatory department   (Registration, QA, QPPV and QP, for own batch release).

Excellent continuous working contacts with the Ministry of Health:

• Fast approvals of new applications within 12 up to 18 months,
• Resolutions of any pending regulatory or quality issue in a professional and credible manner.
• Sole responsibility for the expected registration costs & costs for submission to the Health basket.
• Legal Follow Up – whenever needed, a professional follow up of leading lawyers, specializing in the Pharma Business.