What to report. You must report the information about each obligating action that the submission instructions posted at xxxx://xxx.xxxx.xxx specify.
What to report. The Recipient agrees to report the requisite information about each obligating action required by the submission instructions posted at xxxx://xxx.xxxxxxxxxxx.xxx.
What to report. The award recipient must report the information about each obligating action that the submission instructions posted at XXXX.xxx specify.
What to report. The grant award recipient must report the information about each obligating action that the submission instructions posted at xxxxx://xxx.xxxx.xxx specify.
What to report. You must report the information about each obligating action that the submission instructions posted at http://www.fsrs.gov specify.
What to report. 2.4.1 General Rules on Sales Reporting The rules listed below are applicable to reporting sales to your customer type. Rules specific to your Manufacturer On-site Store is listed in Section 2.4.2. See Exhibit A for rules on pricing for your Manufacturer On-site Store. APPENDIX A Commercial Distillery – Reporting Requirements and Procedures
What to report. Please report any suspected adverse event that your patient(s) may be experiencing, in particular: • serious reactions (e.g. resulting in hospitalisation) • unexpected reactions (reactions not consistent with consumer medicine information or labelling) • all suspected reactions to medicines recently introduced in Australia • all suspected adverse events that may be caused by combinations of medicines (drug interactions) • faults with medical devices resulting in an adverse event (keep the faulty equipment until you have contacted the TGA). What to include in your report In your report include (if applicable): • basic details of the patient experiencing the adverse event – initials, date of birth, gender • details of the adverse event or reaction – date it occurred, symptoms experienced (including duration), description of device fault resulting in adverse event, treatment required and outcome (if known) • details of the medicine or device involved – name, description, dose, for a complementary medicine include AUST L number • details of any other medicine(s) the patient experiencing the adverse event may be taking. Report a medicine or medical device adverse event to the TGA How to report Report a suspected adverse event directly to the TGA using: • GuildCare’s Adverse Events Recording module, sent electronically via a web service portal direct to the TGA • the TGA website - xxxx://xxx.xxx.xxx.xx/xxxxxx/xxxxxxx.xxx Alternatively: Medicines Phone: 0000 000 000 or 0000 000 000 Email: xxx.xxxxxxx@xxx.xxx.xx Medical devices Phone: 0000 000 000
What to report. The Contractor must report the information about each obligating action that the submission instructions posted at xxxx://xxx.xxxx.xxx specify.
What to report. The Indian Tribe agrees to report the information about each obligating action that the submission instructions posted at xxxx://xxx.xxxx.xxx specify.
What to report. You must report the information about each obligating action that the submission instructions posted at xxxx://xxx.xxxx.xxx specify. Draft
