Research Institute For Tropical Medicine, Doh Tender

Description Request For Quotation Mode Of Procurement: Small Value Procurement Date: _____________ Pr No.: _____________ Rfq No.: _____________ Company/business Name: Complete Office Address: Business/mayor’s Permit No: Tin: The Research Institute For Tropical Medicine – Department Of Health, Through Its Bids And Awards Committee (bac), Intends To Procure The Below Mentioned Items Through The Above-mentioned Mode Of Procurement Based On The 2016 Revised Implementing Rules And Regulations Of Republic Act No. 9184. Please Quote Your Best Offer For The Item/s Described Herein, Subject To The Terms And Conditions Provided On This Request For Quotation (rfq). Submit Your Quotation Duly Signed By You, Or Your Duly Authorized Representative Within Five (5) Days Which Shall Be Addressed To The Ritm Bids And Awards Committee. A)the Following Documents Are Required To Be Submitted Along With Your Formal Quotation: Documentary Requirement Remarks Valid And Current Mayor’s/business Permit In Case Not Yet Available, You May Submit Your Expired Mayor’s Or Business Permit With The Official Receipt Of Renewal Application. However, A Copy Of The Latest Mayor’s Or Business Permit Shall Be Required To Be Submitted After Award Of Contract But Before Payment. Valid And Current Certificate Of Platinum Membership With Valid Annex “a” May Be Submitted In Lieu Of The Mayor’s/business Permit Philgeps Registration/membership Bir Form 2303 Company Name Registered In Sec/dti/cda Must Be The Same Registered Name In Bir Form 2303. B)the Following Documents Shall Be Submitted By The Bidder Before The Issuance Of Notice Of Award: Documentary Requirement Remarks Duly Notarized Revised Omnibus Sworn Statement (10 Provisions) With Latest Rules On Notarial Practice Applicable For: Np-svp With Abcs Above P50,000.00 And Np-ec With Abcs Above P500,000.00 Note: Othe Pr # Shall Be Reflected In The Omnibus Sworn Statement Oone (1) Original Copy Must Be Submitted Othe Issuance And Notarial Date Of The Omnibus Sworn Statement Shall Be The Same/after The Issuance And Notarial Date Of The Authority Of The Signatory. Othe Authorized Representative Declared In The Omnibus Sworn Statement Shall Be In Congruent With The Submitted Authority Of The Signatory. Authority Of The Signatory Applicable For: Np-svp With Abcs Above P50,000.00 And Np-ec With Abcs Above P500,000.00 for Sole Proprietorship – Duly Notarized Special Power Of Attorney, If Signatory Is Other Than The Owner for Corporation – Duly Notarized Secretary’s Certificate for Partnership, Cooperative, Or Joint Venture – Duly Notarized Board/partnership Resolution, Whichever Is Applicable Note: Othe Pr # Shall Be Reflected In The Authority Of The Signatory Oone (1) Original Copy Must Be Submitted Othe Issuance And Notarial Date Of The Authority Of The Signatory Shall Be The Same/shall Come First Before The Issuance And Notarial Date Of The Omnibus Sworn Statement. Note: Incomplete Submission Of The Required Documents Will Be A Ground For Disqualification. For Any Clarification, You May Contact Us At The Contact Information Provided: Mae Marie E. Hernandez Bac Secretariat Head (632) 8807-2628 To 32 Loc. 210 And/or 240 E-mail Address: Procurement@ritm.gov.ph / Procurement_02@ritm.gov.ph Website: Www.ritm.gov.ph Instructions: Note: Failure To Follow These Instructions Will Disqualify Your Entire Quotation. (1)do Not Alter The Contents Of This Form In Any Way. (2)the Use Of This Rfq Is Highly Encouraged To Minimize Errors Or Omissions Of The Required Mandatory Provisions. If Another Form Is Used Other Than The Latest Rfq, The Quotation Shall Contain All The Mandatory Requirements/provisions Including Manifestation On The Agreement With The Terms And Conditions Below. (3)all Technical Specifications Must Be Complied With. Failure To Comply With The Mandatory Requirements Shall Render The Quotation Ineligible/disqualified. (4)quotations May Be Submitted Through Electronic Mail At: Procurement@ritm.gov.ph / Procurement_02@ritm.gov.ph. (5)quotations, Including Documentary Requirements, Received After The Deadline Shall Not Be Accepted. For Quotations Submitted Via Electronic Mail, The Date And Time Of Receipt Indicated In The Email Shall Be Considered. Terms And Conditions: bidders Shall Provide Correct And Accurate Information Required In This Form. any Interlineations, Erasures, Or Overwriting Shall Be Valid Only If They Are Signed Or Initialed By You Or Any Of Your Duly Authorized Representative/s. price Quotation/s, To Be Denominated In Philippine Peso, Shall Include All Taxes, Duties, And/or Levies Payable – If Applicable. quotations Exceeding The Approved Budget For The Contract Shall Be Rejected. in Case Of Two Or More Bidders Are Determined To Have Submitted The Lowest Calculated Quotation/lowest Calculated And Responsive Quotation, The Ritm-bac Shall Adopt And Employ “draw Lots” As The Tie-breaking Method To Finally Determine The Single Winning Provider In Accordance With Gppb Circular 06-2005. award Of Contract Shall Be Made To The Lowest Quotation Which Complies With The Technical Specifications, Requirements And Other Terms And Conditions Stated Herein. payment Shall Be Made After Delivery And Upon The Submission Of The Required Supporting Documents, I.e., Order Slip And/or Billing Statement, By The Supplier, Contractor, Or Consultant. Our Government Servicing Bank, I.e., The Land Bank Of The Philippines, Shall Credit The Amount Due To The Identified Bank Account Of The Supplier, Contractor, Or Consultant Not Earlier Than Twenty-four (24) Hours, But Not Later Than Forty-eight (48) Hours, Upon Receipt Of Our Advice. Please Note That The Corresponding Bank Transfer Fee, If Any, Shall Be Chargeable To The Account Of The Supplier, Contractor, Or Consultant. liquidated Damages Equivalent To One-tenth Of One Percent (0.1%) Of The Value Of The Goods Not Delivered Within The Prescribed Delivery Period Shall Be Imposed Per Day Of Delay. Ritm May Terminate The Contract Once The Cumulative Amount Of Liquidated Damages Reaches Ten Percent (10%) Of The Amount Of The Contract, Without Prejudice To Other Courses Of Action And Remedies Available To The Procuring Entity. Technical Offer/proposal: After Having Carefully Read And Accepted The Instructions And Terms And Conditions, I/we Submit Our Technical Proposals/quotations For The Item/s As Follows: Item # Qty/ Unit Item Description Supplier’s Compliance (indicate Brand And/or Model, Including Complete Specifications To Be Offered - Applicable) 1 200/vial/ampule Amikacin (as Sulfate) 250 Mg/ml, 2 Ml Ampul/vial (im, Iv) General Condition And Requirements: 1)product Literature Of The Specific Product Being Offered Indicated In The Bid Proposal; 2)valid Certification/authorization From The Manufacturer/importer/distributor, That The Bidder Is An Authorized/exclusive Distributor Or Dealer Of The Products/items; 3)licenses: •valid And Current Certificate Of Product Registration (cpr) • Valid And Current License To Operate (lto) As Drug Distributor • Valid And Current Lot Release Certificate From Fda (for Vaccines/immunoglobulins/serum) • Valid And Current Certificate Of Gmp From Fda Or From The Manufacturer Issued By The Regulatory Authority Of The Country Of Manufacture 4)copy Of Returns Policy Should Be Submitted Covering Short And Even Longer Shelf-life For All Items. • Valid And Current Batch Notification From Fda (for Anti-infectives) • Certificate Of Analysis (local) For Anti-infectives. • Packaging Instruction: Standard Packaging Of The Manufacturer As Approved By Pfda. • Shelf Life And Replacement: • For Every Delivery, Goods Must Be Fresh Commercial Stock, With A Total Shelf Life Of 24 Months From The Manufacturing Date But Not Less Than 18 Months From The Date Of Delivery. – •for Medicine With Approved Shorter Shelf Life, Replacement For Fresh Stocks Shall Be Issued When Returned Three 3 Months Before Expiry Date. A Guarantee Letter Form The Supplier Shall Be Required As Part Of The Technical Specification Requirement. Additional Requirements For All Items: • Submit Valid And Current Certificate Of Product Registration (cpr) Upon Delivery Delivery Schedule: One Time Delivery (7days Upon Receipt Of Notice To Proceed (ntp)) 2 200/bottle Amoxicillin (as Trihydrate) 250 Mg/5 Ml Granules/powder For Suspension,60 Ml General Condition And Requirements: 1)product Literature Of The Specific Product Being Offered Indicated In The Bid Proposal; 2)valid Certification/authorization From The Manufacturer/importer/distributor, That The Bidder Is An Authorized/exclusive Distributor Or Dealer Of The Products/items; 3)licenses: •valid And Current Certificate Of Product Registration (cpr) • Valid And Current License To Operate (lto) As Drug Distributor • Valid And Current Lot Release Certificate From Fda (for Vaccines/immunoglobulins/serum) • Valid And Current Certificate Of Gmp From Fda Or From The Manufacturer Issued By The Regulatory Authority Of The Country Of Manufacture 4)copy Of Returns Policy Should Be Submitted Covering Short And Even Longer Shelf-life For All Items. • Valid And Current Batch Notification From Fda (for Anti-infectives) • Certificate Of Analysis (local) For Anti-infectives. • Packaging Instruction: Standard Packaging Of The Manufacturer As Approved By Pfda. • Shelf Life And Replacement: • For Every Delivery, Goods Must Be Fresh Commercial Stock, With A Total Shelf Life Of 24 Months From The Manufacturing Date But Not Less Than 18 Months From The Date Of Delivery. – •for Medicine With Approved Shorter Shelf Life, Replacement For Fresh Stocks Shall Be Issued When Returned Three 3 Months Before Expiry Date. A Guarantee Letter Form The Supplier Shall Be Required As Part Of The Technical Specification Requirement. Additional Requirements For All Items: • Submit Valid And Current Certificate Of Product Registration (cpr) Upon Delivery Delivery Schedule: One Time Delivery (7days Upon Receipt Of Notice To Proceed (ntp)) 3 1,500/capsule Cloxacillin (as Sodium Salt) 500 Mg Capsule Amoxicillin (as Trihydrate) 250 Mg/5 Ml Granules/powder For Suspension,60 Ml General Condition And Requirements: 1)product Literature Of The Specific Product Being Offered Indicated In The Bid Proposal; 2)valid Certification/authorization From The Manufacturer/importer/distributor, That The Bidder Is An Authorized/exclusive Distributor Or Dealer Of The Products/items; 3)licenses: •valid And Current Certificate Of Product Registration (cpr) • Valid And Current License To Operate (lto) As Drug Distributor • Valid And Current Lot Release Certificate From Fda (for Vaccines/immunoglobulins/serum) • Valid And Current Certificate Of Gmp From Fda Or From The Manufacturer Issued By The Regulatory Authority Of The Country Of Manufacture 4)copy Of Returns Policy Should Be Submitted Covering Short And Even Longer Shelf-life For All Items. • Valid And Current Batch Notification From Fda (for Anti-infectives) • Certificate Of Analysis (local) For Anti-infectives. • Packaging Instruction: Standard Packaging Of The Manufacturer As Approved By Pfda. • Shelf Life And Replacement: • For Every Delivery, Goods Must Be Fresh Commercial Stock, With A Total Shelf Life Of 24 Months From The Manufacturing Date But Not Less Than 18 Months From The Date Of Delivery. – •for Medicine With Approved Shorter Shelf Life, Replacement For Fresh Stocks Shall Be Issued When Returned Three 3 Months Before Expiry Date. A Guarantee Letter Form The Supplier Shall Be Required As Part Of The Technical Specification Requirement. Additional Requirements For All Items: • Submit Valid And Current Certificate Of Product Registration (cpr) Upon Delivery Delivery Schedule: One Time Delivery (7days Upon Receipt Of Notice To Proceed (ntp)) 4 580/tube Mupirocin Ointment 2%, 5g (tube) Amoxicillin (as Trihydrate) 250 Mg/5 Ml Granules/powder For Suspension,60 Ml General Condition And Requirements: 1)product Literature Of The Specific Product Being Offered Indicated In The Bid Proposal; 2)valid Certification/authorization From The Manufacturer/importer/distributor, That The Bidder Is An Authorized/exclusive Distributor Or Dealer Of The Products/items; 3)licenses: •valid And Current Certificate Of Product Registration (cpr) • Valid And Current License To Operate (lto) As Drug Distributor • Valid And Current Lot Release Certificate From Fda (for Vaccines/immunoglobulins/serum) • Valid And Current Certificate Of Gmp From Fda Or From The Manufacturer Issued By The Regulatory Authority Of The Country Of Manufacture 4)copy Of Returns Policy Should Be Submitted Covering Short And Even Longer Shelf-life For All Items. • Valid And Current Batch Notification From Fda (for Anti-infectives) • Certificate Of Analysis (local) For Anti-infectives. • Packaging Instruction: Standard Packaging Of The Manufacturer As Approved By Pfda. • Shelf Life And Replacement: • For Every Delivery, Goods Must Be Fresh Commercial Stock, With A Total Shelf Life Of 24 Months From The Manufacturing Date But Not Less Than 18 Months From The Date Of Delivery. – •for Medicine With Approved Shorter Shelf Life, Replacement For Fresh Stocks Shall Be Issued When Returned Three 3 Months Before Expiry Date. A Guarantee Letter Form The Supplier Shall Be Required As Part Of The Technical Specification Requirement. Additional Requirements For All Items: • Submit Valid And Current Certificate Of Product Registration (cpr) Upon Delivery Delivery Schedule: One Time Delivery (7days Upon Receipt Of Notice To Proceed (ntp)) Financial Offer/proposal: Please Quote Your Best Offer For The Item/s Below. Please Do Not Leave Any Blank Items. Indicate “0” If Item Being Offered Is For Free: Item # Qty/ Unit Item Description Abc Price Proposal Unit Cost Price Proposal Total Cost 1 200/vial/ampule Amikacin (as Sulfate) 250 Mg/ml, 2 Ml Ampul/vial (im, Iv) General Condition And Requirements: 1) Product Literature Of The Specific Product Being Offered Indicated In The Bid Proposal; 2) Valid Certification/authorization From The Manufacturer/importer/distributor, That The Bidder Is An Authorized/exclusive Distributor Or Dealer Of The Products/items; 3) Licenses: •valid And Current Certificate Of Product Registration (cpr) • Valid And Current License To Operate (lto) As Drug Distributor • Valid And Current Lot Release Certificate From Fda (for Vaccines/immunoglobulins/serum) • Valid And Current Certificate Of Gmp From Fda Or From The Manufacturer Issued By The Regulatory Authority Of The Country Of Manufacture 4) Copy Of Returns Policy Should Be Submitted Covering Short And Even Longer Shelf-life For All Items. • Valid And Current Batch Notification From Fda (for Anti-infectives) • Certificate Of Analysis (local) For Anti-infectives. • Packaging Instruction: Standard Packaging Of The Manufacturer As Approved By Pfda. • Shelf Life And Replacement: • For Every Delivery, Goods Must Be Fresh Commercial Stock, With A Total Shelf Life Of 24 Months From The Manufacturing Date But Not Less Than 18 Months From The Date Of Delivery. – •for Medicine With Approved Shorter Shelf Life, Replacement For Fresh Stocks Shall Be Issued When Returned Three 3 Months Before Expiry Date. A Guarantee Letter Form The Supplier Shall Be Required As Part Of The Technical Specification Requirement. Additional Requirements For All Items: • Submit Valid And Current Certificate Of Product Registration (cpr) Upon Delivery Delivery Schedule: One Time Delivery (7days Upon Receipt Of Notice To Proceed (ntp)) 19,488.00 2 200/bottle Amoxicillin (as Trihydrate) 250 Mg/5 Ml Granules/powder For Suspension,60 Ml General Condition And Requirements: 1) Product Literature Of The Specific Product Being Offered Indicated In The Bid Proposal; 2) Valid Certification/authorization From The Manufacturer/importer/distributor, That The Bidder Is An Authorized/exclusive Distributor Or Dealer Of The Products/items; 3) Licenses: •valid And Current Certificate Of Product Registration (cpr) • Valid And Current License To Operate (lto) As Drug Distributor • Valid And Current Lot Release Certificate From Fda (for Vaccines/immunoglobulins/serum) • Valid And Current Certificate Of Gmp From Fda Or From The Manufacturer Issued By The Regulatory Authority Of The Country Of Manufacture 4) Copy Of Returns Policy Should Be Submitted Covering Short And Even Longer Shelf-life For All Items. • Valid And Current Batch Notification From Fda (for Anti-infectives) • Certificate Of Analysis (local) For Anti-infectives. • Packaging Instruction: Standard Packaging Of The Manufacturer As Approved By Pfda. • Shelf Life And Replacement: • For Every Delivery, Goods Must Be Fresh Commercial Stock, With A Total Shelf Life Of 24 Months From The Manufacturing Date But Not Less Than 18 Months From The Date Of Delivery. – •for Medicine With Approved Shorter Shelf Life, Replacement For Fresh Stocks Shall Be Issued When Returned Three 3 Months Before Expiry Date. A Guarantee Letter Form The Supplier Shall Be Required As Part Of The Technical Specification Requirement. Additional Requirements For All Items: • Submit Valid And Current Certificate Of Product Registration (cpr) Upon Delivery Delivery Schedule: One Time Delivery (7days Upon Receipt Of Notice To Proceed (ntp)) 18,000.00 3 1,500/capsule Cloxacillin (as Sodium Salt) 500 Mg Capsule Amoxicillin (as Trihydrate) 250 Mg/5 Ml Granules/powder For Suspension,60 Ml General Condition And Requirements: 1) Product Literature Of The Specific Product Being Offered Indicated In The Bid Proposal; 2) Valid Certification/authorization From The Manufacturer/importer/distributor, That The Bidder Is An Authorized/exclusive Distributor Or Dealer Of The Products/items; 3) Licenses: •valid And Current Certificate Of Product Registration (cpr) • Valid And Current License To Operate (lto) As Drug Distributor • Valid And Current Lot Release Certificate From Fda (for Vaccines/immunoglobulins/serum) • Valid And Current Certificate Of Gmp From Fda Or From The Manufacturer Issued By The Regulatory Authority Of The Country Of Manufacture 4) Copy Of Returns Policy Should Be Submitted Covering Short And Even Longer Shelf-life For All Items. • Valid And Current Batch Notification From Fda (for Anti-infectives) • Certificate Of Analysis (local) For Anti-infectives. • Packaging Instruction: Standard Packaging Of The Manufacturer As Approved By Pfda. • Shelf Life And Replacement: • For Every Delivery, Goods Must Be Fresh Commercial Stock, With A Total Shelf Life Of 24 Months From The Manufacturing Date But Not Less Than 18 Months From The Date Of Delivery. – •for Medicine With Approved Shorter Shelf Life, Replacement For Fresh Stocks Shall Be Issued When Returned Three 3 Months Before Expiry Date. A Guarantee Letter Form The Supplier Shall Be Required As Part Of The Technical Specification Requirement. Additional Requirements For All Items: • Submit Valid And Current Certificate Of Product Registration (cpr) Upon Delivery Delivery Schedule: One Time Delivery (7days Upon Receipt Of Notice To Proceed (ntp)) 10,350.00 4 580/tube Mupirocin Ointment 2%, 5g (tube) Amoxicillin (as Trihydrate) 250 Mg/5 Ml Granules/powder For Suspension,60 Ml General Condition And Requirements: 1) Product Literature Of The Specific Product Being Offered Indicated In The Bid Proposal; 2) Valid Certification/authorization From The Manufacturer/importer/distributor, That The Bidder Is An Authorized/exclusive Distributor Or Dealer Of The Products/items; 3) Licenses: •valid And Current Certificate Of Product Registration (cpr) • Valid And Current License To Operate (lto) As Drug Distributor • Valid And Current Lot Release Certificate From Fda (for Vaccines/immunoglobulins/serum) • Valid And Current Certificate Of Gmp From Fda Or From The Manufacturer Issued By The Regulatory Authority Of The Country Of Manufacture 4) Copy Of Returns Policy Should Be Submitted Covering Short And Even Longer Shelf-life For All Items. • Valid And Current Batch Notification From Fda (for Anti-infectives) • Certificate Of Analysis (local) For Anti-infectives. • Packaging Instruction: Standard Packaging Of The Manufacturer As Approved By Pfda. • Shelf Life And Replacement: • For Every Delivery, Goods Must Be Fresh Commercial Stock, With A Total Shelf Life Of 24 Months From The Manufacturing Date But Not Less Than 18 Months From The Date Of Delivery. – •for Medicine With Approved Shorter Shelf Life, Replacement For Fresh Stocks Shall Be Issued When Returned Three 3 Months Before Expiry Date. A Guarantee Letter Form The Supplier Shall Be Required As Part Of The Technical Specification Requirement. Additional Requirements For All Items: • Submit Valid And Current Certificate Of Product Registration (cpr) Upon Delivery Delivery Schedule: One Time Delivery (7days Upon Receipt Of Notice To Proceed (ntp)) 72,993.00 Delivery Period: One Time Delivery (7days Upon Receipt Of Notice To Proceed (ntp) Total Offered Quotation In Words: ______________ In Figures: ______________ Price Validity: ________________ Payment Terms: Thirty (30) Calendar Days Payment Details: Banking Institution: _________________________________________________ Account Number: __________________________________________________ Account Name: _________________________________________________ Branch: _________________________________________________ Note: Only The Actual Amount Of The Accepted Items Shall Be Paid. ___________________________ Signature Over Printed Name Of Authorized Representative ___________________________ Position/designation ___________________________ Office Telephone/fax/mobile Nos. ___________________________ Email Address/es