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INTERNATIONAL CONFERENCE ON Harmonization OF TECHNICAL REQUIREMENTS FOR REGISTRATION OF PHARMACEUTICALS FOR HUMAN USE ICH Harmonized TRIPARTITE GUIDELINE PRECLINICAL SAFETY EVALUATION OF BIOTECHNOLOGY-DERIVED
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S6r1 - ich stands for Section 6, Rule 1 - Initial Case Hearing.
The party initiating the legal action is required to file s6r1 - ich.
S6r1 - ich must be filled out completely and accurately with all relevant information about the case.
The purpose of s6r1 - ich is to schedule an initial case hearing and provide necessary information to the court.
S6r1 - ich must include details about the parties involved, nature of the case, and proposed hearing dates.
The deadline to file s6r1 - ich in 2023 is typically set by the court and may vary.
The penalty for late filing of s6r1 - ich may include fines, dismissal of the case, or other sanctions imposed by the court.
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