Mode of Shipment: LCL
Shipping Instructions
  1. In compliance with FDA GMP PIC/S standards for all manufacturing companies, containers of Active Pharmaceutical Ingredients (API) and excipients should bear the following information on the label as shipping marks:
  2. Certificate of Analysis should be in the manufacturer's company letterhead with complete address and contact number, specifications with results, statement of conformance, reference official monograph, and signature of the analyst and approving authority.
  3. Shelf life upon schedule of dispatch should be at least 80%, or follow the shelf life requirement stated in the purchase order. Where specified, remaining shelf life upon dispatch should not be less than 18 months.
  4. Goods to be delivered should come from one (1) batch only, unless otherwise specified in the purchase order.
  5. Kindly furnish in advance a copy of the shipping documents for checking and approval prior to dispatch.
  6. Original copies of the shipping documents such as Invoice, Packing List, Certificate of Analysis, and applicable trade or origin documents should be couriered/sent to:
LLOYD LABORATORIES, INC.
#73 Scout Fernandez St., Brgy. Laging Handa, Quezon City 1103, Philippines
Tel. No.: +632-372-3984 to 89 local 145
Mobile No.: +63 946 900 8240
Contact Person: Ms. Marilou Pangilinan
Trade and Shipping Documents

Please provide the following documents, as applicable:

Preferential Trade Forms

Use the applicable preferential trade form or certificate of origin depending on the country of shipment:

Sea Shipments
LCL Shipments

For less than container load (LCL) shipments, the preferred forwarders and warehouses for cheaper inbound charges are:

LCL guideline: up to 1,000 kg and up to 5 CBM, where applicable.

Non-Compliance

Non-compliance with these instructions would mean non-acceptance of deliveries.

Conforme
Supplier:
Authorized Signature:
Date: